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Novacyt Group

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FY2020 Annual Report · Novacyt Group
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Novacyt Group Annual Report and Accounts for the year ended 31 December 2020

Accelerating 
our strategy for  
long-term value

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Headquarters:
Novacyt Group (UK)  
Unit 1, Watchmoor Point, Watchmoor 
Road, Camberley, Surrey GU15 3AD
T +44 (0) 1276 600 081  
F +44 (0) 1276 600 151  
E investor.relations@novacyt.com

www.novacyt.com

Registered Address: 
Novacyt Group (France)  
13 Avenue Morane Saulnier 78140 
Vélizy-Villacoublay, France
Registered Number: 491 062 527

 
 
 
 
 
 
 
 
 
 
 
 
Business 
Overview

Strategic 
Report

Our 
Governance

Financial 
Statements

Company 
Information

Financial highlights

Revenue £’000 
(2019: £11,468)

£277,204

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Gross Margin £’000 
(2019: £7,340)

£211,500

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EBITDA £’000 
(2019: £174)

£176,145

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Read the financial review 
on pages 26 to 29

Operational highlights

Acquisition 
of IT-IS 

Net Debt £’000 
(2019: £5,567)

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COVID-19 
response

Providing a profitable diagnostic 
instrument development and 
manufacturing company with a solid 
reputation in development of mobile and 
rapid PCR instruments with proven high-
quality, performance and reliability.

The Company experienced 
unprecedented sales demand for its 
COVID-19 products during 2020, which 
transformed our financial position, 
resulting in us significantly exceeding our 
full year 2020 budget and surpassing any 
previous performance.

Contents

Business Overview 

The year that was 2020

Group at a Glance

Business Model

Strategic Report 

Chairman's Statement

Market Opportunity

Our Strategy

Q&A with CEO and CFO

Chief Executive Officer's report

Section 172(1) Statement

Financial Review

Sustainability

Governance

The Board of Directors

The Executive team

Directors’ report

An introduction from the Chairman

QCA principles

Nomination Committee report

Directors’ Remuneration report

Remuneration Committee

Audit Committee report

Principal Risks and  
Risk Management

Financial Statements

Statement of Directors’ 
responsibilities in respect of 
the annual report and financial 
statements

Statutory auditor’s report on the 
consolidated financial statements

Accounts and notes

Consolidated income statement

Consolidated statement of 
comprehensive income

Statement of financial position

Statement of changes in equity

Statement of cash flows

Notes to the annual accounts

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Glossary of terms

Company Information

136

IBC

Novacyt is a diagnostics group, manufacturing 
diagnostic and pathogen testing kits based 
on molecular and protein testing technologies 
sold into human clinical, life science, food and 
industrial markets. 

Leading the response 
to COVID-19 

We developed one of the first tests for COVID-19, achieving 
the CE mark and regulatory approval in February 2020.  
We created new products for COVID-19 throughout 2020. 

Our response to COVID-19 has enabled Novacyt to 
demonstrate the value of the business foundations that have 
been developed during the last few years.

Accelerating our strategy 
for long-term value

We have been able to accelerate our strategy for delivering 
long-term value to Shareholders. We have identified specific 
high-value opportunities for growth in the diagnostics 
market where Novacyt can leverage its innovative position 
for developing new in vitro diagnostic products. In addition, 
with new opportunities created by an increased demand 
for diagnostics and investment in the industry, we expect to 
further boost revenues and profitability through selective and 
accretive acquisitions.

Read more on our COVID-19 response 
on page 3

Read more on accelerating our strategy 
on pages 18 and 19

Read more on the acquisition 
on page 23

Read more on our response 
on pages 22 to 24

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020

01
01

Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNovacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020The year that was 
2020

For many, the year 2020 will always be remembered as the year 
that everything changed. From the way we greeted one another,  
to the way we held meetings, it was truly the year of radical 
transformation for many businesses. 

For Novacyt, we too had a transformational year. From a mid-
sized company of 110 people to a group of 237 people by the 
end of 2020. We have the capability to rapidly innovate new 
solutions and now supply our Gold standard kits to over 130 
countries worldwide. 

The Novacyt ethos has shone through, with 
everyone demonstrating a continued drive and 
positivity to innovate new products rapidly.
As a pioneer in clinical diagnostics, we have a proven history 
of responding quickly to changing global health needs, which 
includes providing testing solutions for Zika, Swine flu, and 
Ebola viruses. Solidifying this position, we were among the first 
to respond to the COVID-19 pandemic in 2020, providing a 
rapid and reliable CE-IVD marked SARS-CoV-2 testing kit.

Breakthrough innovations in 2020 by Novacyt Group

JUL
AWARDED LTA  
WITH UNICEF

MAR
EUA FROM THE 
FDA FOR FIRST 
COVID-19 TEST

APR
EUL FROM WHO 
FOR FIRST COVID-
19-CE IVD TEST

JAN/FEB 
RUO
Product launches
RUO novel Coronavirus test.

genesig®
Product launches
genesig® real-time PCR 
(polymerase chain reaction) 
COVID-19 (CE), the first CE-mark 
approved test for clinical diagnosis 
of the 2019 strain of the novel 
coronavirus.

Market need
In late 2019, researchers in China 
identified a new virus that had 
infected dozens of people in Asia. 
As the COVID-19 pandemic began 
to spread beyond China, the need 
for testing increased exponentially 
worldwide.

JUN 
exsig® DIRECT, 
exsig® and COVID-HT
Product launches
Two new products to support 
laboratories testing for COVID-19. 
These were exsig® Direct and 
exsig® Mag, both RNA extraction kits 
for use prior to running a PCR test for 
COVID-19, and COVID-HT, a high-
throughput test for COVID-19.

Market need
The number of known Coronavirus 
cases across the globe grew rapidly, 
with more than 100,000 new 
infections a day, causing demand for 
higher throughput COVID-19 tests. 
The onset of mass testing globally 
brought about many challenges. One 
of the most profound was a sudden 
shortage of pre-analytical solutions 
required for sample preparation prior 
to PCR testing for COVID-19.

Business 
Overview

Strategic 
Report

Our 
Governance

Financial 
Statements

Company 
Information

SEPT
SARS-CoV-2 IgG EIA
Product launches
CE-mark approved serology (antibody) 
96-well plate ELISA (enzyme-linked 
immunosorbent assay) test for the 
detection of IgG antibodies to SARS-
CoV-2 derived from plasma and 
serum samples.

Market need
Since the onset of the COVID-19 
pandemic, patients and population 
groups have been extensively tested 
for an antibody response to COVID-19. 
Although there is much ongoing 
debate about how the immune system 
responds to different variants, the impact 
of vaccinations and even the type of 
antibody used in the test, our serology 
tests offer additional information on 
a patient profile, supporting ongoing 
population management. 

AUG
Winterplex®
Product launches
Winterplex® CE-mark  
approved PCR respiratory  
test panel.

Market need
With the anticipation of Winter 
in the northern hemisphere, 
Influenza A, B and RSV were 
expected to add complexity to 
the COVID-19 pandemic. 

SEPT
genesig® COVID-19 2G
Product launches
CE-mark approved PCR two-gene  
target test for COVID-19. 

Market need
To support the adoption of our 
products in jurisdictions mandating 
the approach of utilising PCR testing, 
Novacyt’s first generation product 
was improved further with the 
addition of a secondary target to the 
initial Gold standard product.

NOV 
PROmate®
Product launches
PROmate®, a new product to 
improve the workflow efficiency of 
Novacyt’s closer to patient system 
for COVID-19 testing.

Market need
The global death toll from 
coronavirus surpassed 800,000 
in August. The tally continued 
to rise as new infections flared 
across Europe with high numbers 
of deaths recorded in the United 
States, India, South Africa and 
most of Latin America, prompting 
mass testing programmes to 
be operated out of centralised 
laboratories. 

Our contribution 
to the COVID-19 
testing solutions has 
proven that we can 
respond quickly to 
any changing global 
health needs.
Our teams in Marketing and R&D 
aimed to pioneer innovations 
as a strategic priority. We are 
committed to delivering high-quality 
diagnostic products that will make 
a meaningful difference to our 
customers and their patients.

Our state-of-the-art innovations and 
technologies enabled us to be the 
first company globally to respond to 
the threat of the global COVID-19 
pandemic by developing a CE IVD 
molecular test for the virus. Fast 
forward a year: we have developed 
a suite of solutions for COVID-19 
to better manage the pandemic. 
These innovations enable us to 
deploy our expertise in other areas 
of diagnostics, paving the way 
for us to be a truly global clinical 
diagnostics company. 

See page 136 for a  
glossary of terms

02
02

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020
Novacyt Group Annual Report and Accounts for the year ended 31 December 2020
Novacyt Group Annual Report and Accounts for the year ended 31 December 2020

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020
Novacyt Group Annual Report and Accounts for the year ended 31 December 2020
Novacyt Group Annual Report and Accounts for the year ended 31 December 2020

03
03
03

Group at a  
Glance

The Novacyt Group is an international specialist diagnostic solutions 
provider, with a comprehensive product portfolio in advanced 
molecular and protein detection technologies.

Business 
Overview

Strategic 
Report

Our 
Governance

Financial 
Statements

Company 
Information

We passionately believe in providing patient-led focus and 
high-quality innovations, which advance the science behind 
diagnostics in microbiology, haematology and serology testing.

a specialist in the development and 
manufacture of molecular diagnostic 
instrumentation.

focused on design, manufacture, 
validation and supply of Gold standard 
real-time PCR kits, reagents and 
instruments.

IT-IS International 
Acquired by Novacyt in October 
2020, a specialist in the 
development and manufacture 
of molecular diagnostic 
instrumentation, delivers high 
performing technology for real-
time PCR. With comprehensive 
capabilities ranging from molecular 
biology to software engineering, IT-
IS provides products from bespoke 
system development to off the shelf 
real-time PCR machines.

Our capabilities
High quality analysis techniques to 
both real-time PCR amplification 
quantification, and PCR melt 
analysis. Our unique techniques 
identify PCR features such as 
dye response, baseline offset and 
drift, efficiency to yield accurate, 
reproducible results, and to 
recognise potential problem 
samples.

Our products
Agile, portable and high-performing 
real-time PCR instruments:

•  genesig® q16 and q32: 

Novacyt’s exclusive real-time 
PCR machines that work with 
solutions like VersaLab™ to 
provide rapid closer-to-patients 
testing. 

•  MyGo PCR Systems: real-time 
PCR machines that provide 
rapid, precise, quantitative PCR 
and melting point analysis.

Lab 21 Healthcare
Cost-effective solutions in the 
production and distribution of 
reagents and test kits for both IVD 
and blood grouping application.

Our capabilities
Constantly improving production 
efficiency in our attempts to offer 
our end users the most cost-
effective solutions with scale-up 
capabilities. Product improvement 
and enhancement to meet the 
needs of developing markets to 
broaden our geographical market 
coverage.

Our products
Well known for Plasmatec and 
Biotec branded products:

•  Plasmatec: Core products are in 
the areas of latex microbiology 
and serology, blood grouping 
antisera, syphilis serology, and 
pregnancy testing.

•  Biotec: Comprehensive range 

of diagnostic reagents, test kits, 
and blood grouping reagents.

Primerdesign
Focused on the design, 
manufacture, validation, and supply 
of Gold Standard real-time PCR kits 
and reagents. Provides the best 
custom qPCR assay development 
service in the world. Solidifying 
this position, we were among the 
first to respond to the COVID-19 
pandemic in 2020, providing a rapid 
and reliable CE-IVD marked SARS-
CoV-2 test kit.

Our capabilities
Bespoke and commercialisation of 
real-time PCR with an agile team 
that can deliver to market in the 
shortest possible time. 

Our products
Proud producers of Gold Standard 
real-time PCR kits with world-class 
innovations:

•  genesig®: for Pathogen 

detection,food and water testing, 
veterinary and agricultural testing, 
and more recently the COVID-19 
pandemic.

•  PROmate®: total workflow 

solution that is nearer to patients, 
inclusive of sample preparation, 
qPCR amplification, and analysis 
on the genesig® q16 and q32 
instruments, specifically for the 
detection of SARS-CoV-2.

•  SNPsig®: detect SARS-CoV-2 
variants of concern under 2 
hours, designed to run on central 
laboratory systems and the 
genesig® q16 and q32 rapid 
PCR systems.

Microgen Bioproducts
Clinical product range that  
supports healthcare providers in 
improving patient health with a 
comprehensive food diagnostic 
range that helps manufacturers 
ensure consumer safety.

Our capabilities
Expertise in the development, 
manufacturing, distribution, and 
marketing of products used by 
clinical laboratories to detect 
and diagnose infectious disease, 
and by food laboratories to 
detect and identify pathogenic 
organisms. Our product range 
comprises a comprehensive list of 
quality diagnostic solutions in the 
fields of microbiology, serology, 
haematology, bacteriology,  
and virology.

Our products
Recognised leaders in diagnostics 
solutions for infectious diseases 
as well as for food and industrial 
microbiology:

•  PathFlow® Rapid Tests: 

complete solution for the rapid 
diagnosis of infectious diseases 
including for the detection of 
SARS-CoV-2 antibodies.

•  Path-Chek Hygiene Tests: 

detection of a range of bacteria 
from work surfaces and the 
processing environment.

•  Latex Agglutination Kits: simple 
one-step identification and 
confirmation of a range of 
pathogenic bacteria.

a product range of diagnostic 
products in the fields of microbiology, 
serology, haematology, bacteriology 
and virology.

manufacturer and supplier of Plasmatec and 
Biotec branded products, plus a range of 
reagents and tests for IVD application and 
blood grouping.

04

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020

05
05

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Business  
Model

Key resources

Speed to develop 
products
As one of the first diagnostic companies 
to have a launched CE-mark COVID-19 
tests approved by both the FDA and 
the WHO under the Emergency Use 
Listing (“EUL”), Novacyt put itself on the 
map. This product has now received 
regulatory approval from 57 countries. 
As the pandemic has evolved, Novacyt 
has continued to be at the forefront of 
new product development, improving 
workflow with PROmate® for near 
patient testing and tackling new Variants 
of Concern (“VOC”) with SNPsig®. Our 
technology covers a range of PCR, 
ELISA, lateral flow antibody and antigen 
tests for near patient, central labs and 
high throughput settings that can run on 
many laboratory systems, as well as our 
own q16 and q32 rapid-PCR systems. 
Novacyt launched 14 new COVID-19 
related products during 2020.

Manufacturing scale-up
Novacyt revenue increased by over 
20 times from 2019 to 2020. This 
increase in revenue did not occur 
evenly throughout 2020, which meant 
that manufacturing had to scale-up 
even more than the revenue increase. 

This was further compounded by the 
introduction of new products with 
almost 60% of our revenue coming 
from products launched after the 
original COVID genesig® product. 
Novacyt has managed a network of 
sub-contractors to access additional 
capacity, which has accelerated the 
scale-up, ensuring we can flex capacity 
upwards and downwards in line with 
very unpredictable demand patterns. 

Rapid commercialisation
Novacyt has used its extensive network 
of distributors to bring products to 
market consistently and more quickly 
than our competition. We have 
strengthened the commercial leadership 
both internationally and in the UK, to 
drive more direct customer sales and 
build an installed instrument base. In 
the first half of 2021, we have seen a 
shift from Government testing to private 
testing as parts of the economy reopen, 
and we have worked closely with 
several leading private test companies 
in this space including the launch of our 
own mobile trailer solution under the 
VersaLab™ brand. 

Can-do culture
The DNA of Novacyt is an agile 
entrepreneurial business where speed 
to market and indeed speed to patient 
is paramount. The success of 2020 
is testimony to this can-do culture 
in action where significant scientific, 
regulatory and supply chain challenges 
were conquered. As we scale-up the 
organisation, we are preserving our 
core values to ensure we continue 
to respond in a rapidly changing 
environment. 

Innovation
In Novacyt, innovation is about 
delivering effective solutions ahead of 
our competitors. Innovation is where 
all our attributes of speed to develop 
products, manufacturing scale-up and 
rapid commercialisation come together, 
propelled forward by our can-do 
culture. Innovation is only successful 
when all our capabilities combine and 
complement each other. In a market 
with unprecedented opportunities 
developing at pace, Novacyt is in a 
great position to build a sustainable 
long-term business.

Key activities

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INNOVATION

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Environm e n t

Evidencing our outcomes

The financial outcomes for 2020 
show a highly profitable business that 
experienced extraordinary growth 
throughout the year. Beneath the 
headline numbers, we focus on specific 
metrics for our stakeholders:

•  Sales growth of >20 times; EBITDA 
margin of 64%; cash position of  
£92 million; debt free

•  Employee increase from 110 to 237. 
11% staff turnover and no reported 
injuries

•  14 new products launched; 

•  Implementing systems to track 

over 20 patents filed 

customer satisfaction

•  Integration of IT-IS acquisition

06

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Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNovacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Business  
Model continued

Value for stakeholders

Patients
We will continue to produce testing 
kits that are valuable for patient 
management, and give pragmatic 
results that can influence healthcare 
decisions and not simply confirm 
clinical impressions. We commit to 
bring innovations to markets that can 
impact on the management of patients 
and patient care outcomes, which 
are influenced by both specificity and 
sensitivity of our kits. We are proud to 
have played a part in bringing COVID-19 
under control and, equally, the role we 
have played in reopening the economy 
in many areas from film sets, to sporting 
events to fitness for travel. 

Customers
Providing a full range of COVID-19 
diagnostic testing kits that are continually 
updated to reflect latest Variants of 
Concern, developments on single, 
double, or triple gene assays and 
relevant delivery systems from high 
throughput to near patient, covering 
PCR, lateral flow antigen and antibody 
solutions. This flexibility has expanded 
our range of customers considerably 
from public hospitals and central 
laboratories, to private testing and 
mobile labs in numerous patient and 
user settings. We have continued to 
develop ways to make it easier for 
customers to use our products with a 
focus on workflow and instrumentation 
including the acquisition of IT-IS during 
the course of 2020. 

Employees
We understand that our workforce is 
our most valuable asset that sets us 
apart from our competitors. We are 
proud of the role that our employees 
have played throughout the pandemic, 
working like many other industries 
in difficult circumstances. We are 
committed to creating an excellent 
working environment for our employees, 
promoting positive cultures and values 
within a safe workplace. We are also 
committed to diversity and inclusion, 
which we demonstrate through our 
efforts to reduce barriers to success 
where we aim to recruit, retain and 
promote the best people in our sector.

Shareholders
We are committed to creating a 
sustainable and profitable diagnostics 
business with recurring revenues, 
continuing to play a significant role in 
the fight against COVID-19 but also 
expanding our test menu beyond 
COVID-19. We will invest in expanding 
the footprint of our business by 
increasing our installed base of q16 
and q32 machines, and expanding 
geographically, both organically and 
by acquisition where it makes sense 
to do so. We will maintain the highest 
standards of governance to ensure that 
Shareholders’ rights and interests are 
properly considered and protected.

Environment
As Novacyt has grown rapidly during the 
course of 2020 we have also increased 
our focus on Environment, Social and 
Governance (ESG) matters. This has 
meant putting the reporting metrics in 
place to measure our carbon footprint 
and to create action plans to pro-
actively reduce packaging, water and 
energy consumption. We have included 
a separate Sustainability report in this 
years Annual Report for the first time that 
highlights the key performance metrics 
and initiatives. In addition our employees 
have been very active on a broad social 
agenda, working with schools and 
charities to ensure we give some time and 
resources back to the communities we 
work in. This is another part of Novacyt’s 
exciting journey and we are looking 
forward to accelerating our momentum 
throughout 2021 and beyond. 

08

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Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNovacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Building 
on strong 
foundations

Our response to COVID-19 built our 
reputation in the market and has grown our 
strategic relationships and customer base.

Read more about our strategy 
on pages 18 and 19

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1111

 
Chairman’s 
Statement

Last year I started by saying that “I am writing this report in 
unprecedented times”. This statement remains true today and 
despite the human difficulties associated with the incredibly 
challenging conditions that we have all faced over the last year, 
the business has undergone transformational change during 
2020 and has been at the heart of providing testing capability 
both in the UK and in over 130 countries worldwide. 

James Wakefield
Chairman

Due to the nature of our business 
and our highly experienced staff, we 
were able to benefit from first mover 
advantage by developing a reliable test 
for COVID-19 quickly. This received 
worldwide recognition and approval in 
57 countries and enabled us to continue 
to develop further products in our test 
portfolio as more and more strains of the 
virus materialised. 

We rose to the challenge of significantly 
increasing production capacity through 
a massive scale up internally as well as 
outsourced production whilst retaining 
overall control of the process. In the UK, 
we worked in close partnership with the 
UK Department of Health and Social 
Care (“DHSC”) as well as with a number 
of other customers worldwide. At times, 
weekly demand levels were greater than 
we had historically seen in a year.

I want to publicly thank every member 
of our team for their superb contribution 
and for going “above and beyond” what 
is normally expected. I also want to thank, 

once again, their families for making 
this possible. Every situation is different 
and I know that at one time or another, 
significant sacrifices have been made by 
everyone.

We remain focussed on the Group’s 
profitable reagent development and 
manufacturing business units, which we 
consider to be the key long-term value 
drivers of the business.

At the start of 2020, the business 
repositioned its focus to be at the heart 
of supporting the global pandemic 
with its COVID-19 test. Our rapid 

2020 highlights

•  Profitable after tax for the first 
time in the Company’s history 
with all senior debt repaid  
by H2

•  Net consideration for 

acquisition of IT-IS after 
earnouts was £8.7m,  
100% out of cash-flow

•  Providing testing capability 
for COVID-19 in over 130 
countries around the world

Read more on corporate 
governance on pages 36 to 56

Read more in the financial 
review on pages 26 to 29

response to this latest COVID-19 virus 
outbreak is a testament to the Group’s 
core competency of in-vitro diagnostic 
design, development, manufacturing 
and commercialisation, and being able 
to act quickly. I am extremely proud of 
the Novacyt team who were able to 
deliver this new COVID-19 test in such 
a short period of time for our customers 
who continue to need fast and reliable 
diagnostic solutions.

During the 2020 period under review, we 
generated revenues of £277m and a net 
profit for the first time in the company’s 
history. By the half year point, all senior 
debt had been repaid and the Group 
continued to increase its cash reserves 
to have over £91m by the year end after 
financing the £8.7million acquisition of 
IT-IS. We look forward to continuing to 
expand into new international markets 
and can do this from a materially stronger 
financial position as a result of the 
exceptional performance during 2020. 
Regrettably, we now find ourselves in 
a dispute with the DHSC, our largest 
customer in 2020, which is explained in 
the financial section of this report. Overall, 
however, this has been a transformational 
year for the business and as I write this 
report, the valuation is over 20 times 
higher than it was at the start of 2020 and 
the business is debt free.

We are delighted to be working with 
Allegra Finance as our French listing 
sponsor, SP Angel Corporate Finance LLP 
as our Nominated Adviser/ Broker, and 
added Numis as well during 2020.

The Board has reviewed and reconfirmed 
its strategy to continue to focus on its 
core strengths of in-vitro diagnostic 
product development, commercialisation 
and contract manufacturing by driving 
value from our profitable Primerdesign 
and Lab21 businesses. It is the intention 
to continue to grow both organically and 
through selective acquisition. 

We are not proposing to pay a dividend 
for the financial year ended 2020 so we 

Revenues of 

£277m

in 2020

Over

£91m

cash at end of 2020

James Wakefield

Chairman

can invest in R&D, manufacturing and 
commercial aspects of the business. In 
the future, our dividend policy will form 
part of a wider review of capital allocation, 
which will be formulated in conjunction 
with the requirements for continued 
investment in the business for future 
business growth to maximise shareholder 
value as well as the prevailing financial 
conditions in the markets in which the 
business operates.

The Company is listed on two stock 
exchanges: Euronext Growth Paris 
and AIM London. As such, the Board 
remains committed to maintaining the 
highest standards of transparency, 
ethics and corporate governance, whilst 
also providing leadership, controls and 
strategic oversight to ensure that we 
deliver value to all our stakeholders.

Finally, I would like to take this opportunity 
of thanking you, the shareholders, for your 
continued support, and also to thank the 
Board, the Executive management team 
and all of our staff for their commitment 
and contribution to the business and, in 
particular, to the role that Novacyt has 
and continues to have in testing during 
this global pandemic.

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Opportunity

The IVD market 
The global COVID-19 pandemic has transformed the need for 
early diagnosis, increasing the demand for diagnostics kits and 
assays to unprecedented levels. Looking forward, it is likely that 
we will see elevated levels of demand for years to come. 

Projected diagnostics market growth1:

5.10%

4.82%

23.40%

25.20%

Market size in 2020 (inner): US $69.52 billion
Market size in 2030 (outer): US $113.86 billion

■ Software 
■ Instruments
■ Consumables

Impact analysis on the global IVD market

69.98%

71.50%

Adoption of rapid, minimally invasive,  
and non-invasive diagnostics

1–2 Years

3–5 Years

6–10 Years

High

Medium/High

Medium/High

Rise in the global geriatric population

Medium/High

Medium/High

Medium/High

Global IVD market (by application)1:

Increase in the number of patients with  
infectious and chronic diseases

Medium/High

Medium/High

Medium/High

Rise in the demand for point of care testing

High

Medium

Medium

3.50%

5.50%

9.10%

6.16%

10.70%

Uneven reimbursement scenario

Medium/High

Medium/High

Medium

Uncertain regulatory environment

High

Medium

Low/Medium

11.30%

11.73%

3.00%

3.04%

19.97%

19.10%

25.40%

23.19%

17.27%

18.70%

s
r
e
v
i
r
d
t
e
k
r
a
M

s
e
g
n
e

l
l

a
h
c

t
e
k
r
a
M

* The table above reflects the Company’s view on main market drivers.

Market size in 2020 (inner): US $69.52 billion
Market size in 2030 (outer): US $113.86 billion

■ Diabetes
■ Infectious diseases
■ Oncology/cancer
■ Cardiology and blood disorders
■ Nephrology
■ Immune diseases
■ Drug testing
■ HIV/AIDS
■ Womens Health
■ Others (blood donor screening and human antigen testing)

Global IVD market (by application)1:

24.90%

26.70%

Market size in 2020 (inner): US $69.52 billion
Market size in 2030 (outer): US $113.86 billion

■ Central laboratories
■ Point of care (POC)
■ Clinics
■ Academic institutes
■ Hospitals
■ Others (diagnostic centres and clinical research organisations “CROs”)

31.80%

35.50%

25.70%

29.00%

7.10%

9.30%

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Market  
Opportunity continued

In vitro diagnostics (“IVD”) for human 
clinical diagnosis is a highly fragmented, 
high-growth, high-margin industry with 
high barriers to entry as a result of the 
technology base of the major industry 
players and the regulatory environment. 

The market drivers of growth include the 
need to provide IVD diagnostic results 
faster, more easily and nearer to the 
patient. The unprecedented demand 
for COVID-19 testing has fuelled these 
drivers and significant levels of new IVD 
innovation is expected to be an outcome 
of COVID-19. 

The IVD regulatory barrier is also set to 
increase across Europe in 2022 and other 
countries that rely upon the CE mark 
due to the introduction of the new IVDR 
regulations, which require Notified Body 
approval of more than 80% of all IVD 
diagnostics compared to only 20% today. 
In 2020, it was estimated that the global 
IVD market would grow at a compound 
annual growth rate (“CAGR”) of 5.6% from 
2020–25 with the estimated market size to 
be at US $70 billion in 2020.1 This forecast 
was calculated before the full impact of 
COVID-19 testing was known, so the size 

of the overall IVD market is expected to be 
significantly higher than this. 

The demand for molecular testing, which 
is regarded as the Gold standard for 
diagnosing infectious disease significantly 
increased as COVID-19 testing grew from 
the global pandemic. Industry players 
have responded to this demand by 
innovating and automating IVD systems 
for laboratories and hospitals to provide 
efficient, accurate diagnoses with high 
sensitivity and specificity. 

For most of the first half of 2020, the 
demand for COVID-19 testing far 
exceeded supplies from the diagnostics 
industry and this forced all infectious 
disease focused diagnostic manufacturers 
to rapidly invest in the development and 
scale-up of COVID-19 products. As the 
virus continued to spread and evolve 
with mutations and the market needs for 
near patient testing, as well as central 
laboratory testing, IVD manufacturers 
have been designing kits that are easy 
to use, faster sample to result, and 
flexible enough to detect variants. As the 
pandemic has progressed, the market 
demand for lateral flow tests (“LFT”), 

which are considered less accurate 
than PCR test performance but are 
more convenient to use, has increased 
significantly as Governments wrestle with 
the challenge of opening up economies. 

Beyond COVID-19, the prevalence 
of various diseases such as cancer, 
autoimmune diseases, and inflammatory 
conditions is escalating globally and is 
expected to boost demand for IVD, with 
the infectious disease segment dominating 
the market at 23% in 2020.2

To strengthen manufacturing capacities, 
product pipelines, and competitive 
differentiations, companies are rapidly 
acquiring capabilities through internal 
development, partnerships and M&A.

References: 

1  Market Data Forecast. Global  

In Vitro Diagnostics Market Size. 

Available from:  
www.marketdataforecast.com/market-reports/
global-in-vitro-diagnostics-market.

2  Grand View Research. In Vitro Diagnostics 

Market Size, Share & Trends Analysis Report 
By Product, By Application, By Technology 
(Immunochemistry, Molecular Diagnostics), 
By End-use, By Region, And Segment 
Forecasts, 2021 – 2027.

Available from:  
www.grandviewresearch.com/industry-
analysis/in-vitro-diagnostics-ivd-market.

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Strategy

Build on our success in COVID-19 testing to expand test menus 
in areas adjacent to COVID-19, and then into other prioritised 
market segments, delivery systems and geographies.

Test Menu Expansion

Instrument Expansion

Geographic Expansion

Business 
Overview

Strategic 
Report

Our 
Governance

Financial 
Statements

Company 
Information

…underpinned by compelling IVD market dynamics

Build on Novacyt reputation 
for quality and innovation 
based upon its ability 
to rapidly develop new 
diagnostic reagents. Well 
positioned with one of 
the most comprehensive 
research use only PCR 
menus in the world and over 
60 CE Mark approved clinical 
diagnostics tests which will 
continue to grow through this 
strategy. 
Test menu expansion
•  COVID-19 testing - Continue to 

expand Novacyt’s COVID-19 test 
menu to include additional COVID 
variants as they are identified and 
any reagent innovations which 
support testing efficiencies and 
results delivery. 

•  COVID-19 Plus testing - Targeted 

menu expansion into closely adjacent 
areas of COVID-19, e.g., Flu A, Flu 
B, biomarker monitoring to predict 
COVID progression / response to 
treatments (e.g., IFI27 biomarker 
for COVID-19 disease severity) to 
diagnose conditions in infected / 
recovered patients (e.g., factors 
related to “long COVID”).

•  Post-COVID testing - Addressing 
unmet testing needs beyond 
COVID-19 building on its support 
for established central lab 
customer base with high value 
test menus, such as pathogens 
resistant to antimicrobials 
(e.g., Carbapenemresistant 
Enterobacteriaceae), sepsis, 
transplantation (CMV, EBV, BKV) as 
well as building test menu for its near 
patient strategy.

Underpinned by our strong 
bioinformatics and test design expertise 
coupled with extensive regulatory 
capabilities.

The acquisition of IT-IS 
has provided Novacyt with 
a strong mid-throughput 
near-patient PCR testing 
platform with the q16 and 
q32 instruments which are 
being deployed in multiple 
near patient markets for use 
in COVID-19 testing.
•  Expand placements of q16’s and 

q32’s and build out the specific test 
menu beyond COVID-19 based on 
the use-case requirements of the 
various placements.

•  Develop multiple tests (multiplexing) 
leveraging the Company’s core 
expertise in chemistry development 
coupled with its near patient 
instrumentation technology.

•  Estimated global market size of $69.5 billion in 2020(1) 
with the IVD industry set to experience steady growth 
and continued consolidation

•  Growing at a 5-year CAGR of 5%, with some analysts 

expecting IVD market to top $114 billion by 2030

•  Increased technological innovation

•  Rising living standards in developing countries

•  Industry consolidation

•  An increase in incidence of chronic and infectious 

diseases

•  Aging world population

•  Follow the shift towards further 

decentralised testing through the 
development of high utility tests in 
areas including infection control (e.g., 
Norovirus, C. Diff) sepsis differentiation 
meningitis and neonatal differentiation 
(e.g., Echovirus; Listeria).

•  Further expand decentralised testing 
opportunities through protein based 
diagnostic technologies including 
lateral flow which will be developed, 
licensed or acquired by the Company.

Novacyt has invested heavily 
in the UK with over 40 
people in sales, field support 
activities and marketing, 
which puts the Company in a 
strong competitive position.  
This direct sales model will 
be replicated in selected 
target markets overseas.

•  Geographic expansion particularly 

with a focus in direct sales, 
marketing and distribution beyond 
the UK.

•  Focus on organic and acquisition 

investments.

•  High priority geographies include the 
US, Germany and other European 
markets.

•  Targeted organic investment has 

already commenced in the US with 
the recent appointment of a US 
General Manager.

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CEO and CFO

Business 
Overview

Strategic 
Report

Our 
Governance

Financial 
Statements

Company 
Information

3. How has the integration 
of IT-IS gone and what 
are Novacyt’s future 
acquisition priorities?
The acquisition of IT-IS International 
went smoothly and provides a profitable 
diagnostic instrument development and 
manufacturing company, in line with the 
Group’s strategy. IT-IS has established a 
solid reputation in development of mobile 
and rapid PCR instruments with proven 
high quality, performance and reliability, 
which strengthens Novacyt’s position 
to fulfil the growing market demands for 
rapid near-patient testing of COVID-19,  
as well as other infectious diseases. 

4. What was your 
proudest moment during 
2020?
It is very difficult to answer as 2020 
was a truly challenging, dynamic and 

transformative period for Novacyt with 
many ‘eureka’ moments throughout 
the year. However, one of my proudest 
moments was being invited by 
AstraZeneca, GlaxoSmithKline (“GSK”) 
and the University of Cambridge early 
on in the pandemic to join them in the 
design, development and operating of a 
new COVID-19 testing operation, which 
was later to be sited within Cambridge 
University. This collaboration resulted 
in over 3.8 million COVID-19 PCR tests 
being performed to support the UK’s 
national testing efforts and new testing 
work flows and test reagents being 
created in record time to meet the 
demands of the laboratory. This is a great 
example of how UK Life Sciences came 
together across sectors to work towards 
a common national cause.

Graham Mullis 
Chief Executive Officer

1. How would you 
summarise Novacyt’s 
performance during 
FY20?
The pandemic was an opportunity for 
Novacyt to help people across the globe. 
Novacyt reacted quickly in response to 
the COVID-19 outbreak with our expertise 
in R&D and innovation shining through, 
proving our capabilities as an international 
specialist in clinical diagnostics. This has 
transformed the business with revenues 
for the full year having increased by 
over 20x, gross margin of 76.3% and a 
cash balance of £91.8 million as at 31 
December 2020.
2. What is the focus for 
Novacyt’s R&D investment 
for FY21 and beyond? 
Novacyt will continue to expand its 
menu of next generation COVID-19 
products and closely adjacent areas 
along the COVID patient continuum. 
Beyond COVID, Novacyt will focus on 
addressing unmet needs with high-value 
test menus, such as panels to screen 
for pathogens resistant to antimicrobials. 
In parallel, Novacyt will support the shift 
towards decentralised testing through the 
development of high-utility tests in areas 
like infection control, sepsis differentiation, 
meningitis and neonatal differentiation.

20
20

James McCarthy
Chief Financial Officer

1. What is the strategic 
direction for Novacyt?
As referenced in our strategy update 
on pages 18 and 19, we will maintain 
our leadership in COVID testing whilst 
looking to build a sustainable future 
beyond COVID. We have identified 
specific high-value growth opportunities 
in the diagnostics market where Novacyt 
can leverage its innovative position 
for developing new in vitro diagnostic 
products. We will add new multiplex 
instrument technologies with rapid 
sample to result to support near-patient 
clinical decision making. We will build 
on our international reputation to build 
direct sales channels in targeted priority 
countries through a combination of 
organic investment and M&A, should 
suitable opportunities arise.

2. How do you think the 
diagnostics market will be 
changed by COVID-19?
First of all, we believe that the COVID-19 
virus will remain a challenge for the next 
couple of years as we are likely to be 
exposed to further waves. Hopefully, 
vaccination will make future waves far 
less deadly; however, we will also see 

a commensurate increase in economic 
activity and movement of people. This 
will require sustained, elevated levels of 
testing to keep the virus under control. 

Post-COVID-19, more health authorities 
are expected to demand fast and more 
cost-effective diagnostic testing. The 
presence of diseases such as cancer, 
autoimmune diseases, and inflammatory 
conditions is escalating globally and 
is expected to boost demand for IVD 
products, with the infectious disease 
segment of the market dominating at 
41.8% in 2020.1

3. How will Novacyt 
compete against the 
established and very large 
international players in 
diagnostics?
COVID-19 has caused a rapid expansion 
of the overall market, which has provided 
us with many opportunities we did not 
have before. The speed and innovation 
of Novacyt has been a key competitive 
advantage in a market that has been 
rapidly changing as the virus changed, 
vaccines roll out and indeed the types 
of testing being used have changed. 
We have shown our ability to scale up 

our supply chain quickly and to make 
bolt-on acquisitions where we need to 
strengthen capabilities like we did with 
IT-IS. This is a competitive industry, and 
we have the utmost respect for our 
competitors; however, we are confident 
we can continue to build our business 
successfully.

4. Why did you decide to 
join Novacyt?
Novacyt is an exciting company that has 
made a tremendous impact in the fight 
against the COVID pandemic; however, 
it was the people behind this success 
that made the opportunity most attractive 
to me. The company has a very strong 
‘can-do’ culture while taking care of its 
people and the environment in which they 
work, which appealed to my values. It has 
demonstrated its ability to rapidly develop 
diagnostic tools in response to an ever-
changing environment and this positions 
the company well for future growth, 
both in the UK and internationally. This 
transition from a relatively small business 
to an international player is a unique 
opportunity, both professionally and 
commercially, which I find very compelling.

References: 
1 Grand View Research. In Vitro Diagnostics Market Size, Share & Trends Analysis Report By Product, By Application, By Technology (Immunochemistry, Molecular Diagnostics),  

By End-use, By Region, And Segment Forecasts, 2021 – 2027. Available from: www.grandviewresearch.com/industry-analysis/in-vitro-diagnostics-ivd-market.

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Report

2020 key 
achievements:
•  EBITDA profitability of £176 million

•  All outstanding debt obligations 

of £7.1 million settled, making the 
Company debt free for the first 
time in its history

•  Collaboration with AstraZeneca, 

GSK and the University of 
Cambridge to take action to 
support the national effort to fight 
the COVID-19 pandemic

Primerdesign
Revenue £’000

£272,817

Recurring operating  
profit £’000

£177,837

It is with pleasure and pride that we present our progress during 
these challenging times in 2020. It is humbling to know that 
Novacyt has been making a difference to millions of people’s lives 
and continues to be at the forefront of innovative testing during 
the COVID-19 pandemic. Through the successful operational and 
financial foundations laid down over these past few years, there is 
a great opportunity to build a long-term diagnostics business that 
continues to make a difference to people’s lives and, at the same 
time, create long-term Shareholder value. 

Graham Mullis
Chief Executive Officer

The Company experienced 
unprecedented sales demand for its 
COVID-19 products during 2020, which 
transformed our financial position, 
resulting in our Company significantly 
exceeding our full year 2020 budget and 
surpassing any previous performance. 
Our response to the COVID-19 pandemic 
has been outstanding across the 
entire business and this is down to our 
employees. I could not be more proud 
and humbled at how hard everyone 
continues to work during a difficult and 
challenging time across the globe. This 
pandemic is causing havoc with our 
lives and economy in ways that have not 
been seen since the Second World War, 
but Novacyt remains at the heart of the 
response doing our very best to help 
more than 130 countries diagnose and 
manage the spread of the virus and its 
variants that naturally follow. 

The Group achieved an increase in 
revenues of over 20x to £277.2 million, 
with gross margin of 76.3% and EBITDA 
profitability £176 million for the full year 
of 2020. In June 2020, the Company 
was able to settle all outstanding debt 
obligations of £7.1 million in total with 
Harbert European Growth Capital 
(“HEGC”) and Vatel Capital SAS (“Vatel”), 
making the Company debt free for the 
first time in its history. The Company’s 
cash position at 31 December 2020 was 
£91.8 million.

In February 2020, the Company 
produced one of the first CE-mark 
COVID-19 tests for the 2019 strain of 
the novel coronavirus, with approval 
received from both the US Food and 
Drug Administration (“FDA”) and the 
World Health Organization (“WHO”) for 
the test to be eligible for procurement 
under the Emergency Use Listing (“EUL”). 
The EUL is a risk-based procedure for 
assessing and listing unlicensed vaccines, 
therapeutics and in vitro diagnostics 
with the ultimate aim of expediting the 
availability of these products to people 
affected by a public health emergency. 
This product has now received regulatory 
approval from 57 countries.

April was a significant milestone 
month for the Company. As part of 
the UK Government’s five pillar plan to 
increase testing for COVID-19, Novacyt 
collaborated with AstraZeneca, GSK and 
the University of Cambridge to take action 
to support the national effort. Novacyt 
ensured an effective work-flow process 
for COVID-19 within a new testing 
laboratory set up by these partners at the 
University’s Anne McLaren laboratory in 
addition to providing its COVID-19 test to 
generate results data. 

Towards the end of April, Novacyt 
secured a supply contract with the DHSC 
to supply its COVID-19 test for an initial 
term of six months. This partnership 
reinforced Novacyt’s existing support of 

the UK Government’s five pillar plan to 
increase testing for COVID-19. 

The Company’s biggest challenge during 
2020 was, and remains to be, to develop 
the organisation and systems required 
to support scale-up of the business at 
an unprecedented rate. Whilst managing 
to retain our ability to hold onto core 
competitive advantages, such as speed 
to market, and the quality of our products, 
our headcount has increased by more 
than 100 in the last 18 months. 

Manufacturing functions have seen the 
most change, and the largest scale-up 
during the past 12 months. Chartwell 
Consulting continue to assist Novacyt as 
the complexity of this function increases. 
Despite this, the Company continues 
to deliver substantial margins through 
low cost of goods and is continuously 
adapting to the pandemic with new 
products being introduced monthly. 

Our PCR reagent manufacturing 
capacity remains high with capacity 
to scale further. The Company has a 
number of non-financial key metrics that 
management use to monitor, control 
and make decisions balancing demand, 
supply, stock levels, customer service and 

capacity decisions, which are reviewed 
weekly. Multiple QC KPIs are also 
reviewed weekly and a cross-functional 
Material Review Board (“MRB”) is active 
and in control of manufacturing quality.

In parallel with the day-to-day 
management challenges in the current 
pandemic, Novacyt is making good 
progress in developing its strategic plans, 
which includes engaging with potential 
acquisition targets.

In October 2020, The Company 
acquired IT-IS International, a profitable 
diagnostic instrument development 
and manufacturing company for a net 
consideration after earnouts of £8.7m. 
IT-IS is the exclusive manufacturer 
of Novacyt’s q16 and q32 rapid 
PCR instruments. The transaction 
reinforced our new strategy, securing 
key IP, expanding our core capabilities 
in instrument manufacturing and 
strengthening our product offering in 
mobile PCR devices with an immediate 
increase in earnings.

IT-IS has been an important addition to 
the business’s capability and we now 
have a guaranteed supply of many 
thousands of q16 and q32 machines 

and can scale to virtually any level of 
capacity the business could require. The 
deep knowledge of PCR instrumentation 
that comes with IT-IS means we are well 
placed for the development of the next 
generation of machine, the planning of 
which has already begun.

We seek to predict and stay abreast of 
the fast pace of product differentiation 
required in the market to maintain our 
competitive position, and this is evident 
with our rapid development and launch 
of new Variants of Concern (“VOC”) tests 
branded as SNPsig®. To date, Novacyt 
has launched over 14 new COVID-19-
related products since the beginning of 
2020.

In the last 12 months, the business has 
moved from one to three major product 
platforms: 

i.  96 reaction genesig® product for small 

laboratories; 

ii.  PROmate® for near-patient testing; 

and 

iii.  High throughput kits for large 

laboratories. 

All three product platforms have proven 
to be successful and open different 

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Report

continued

potential markets. There are a number of 
other exciting and potentially large new 
business development opportunities that 
could drive major increases in COVID-19 
sales during the remainder of 2021.

Innovative R&D and IP
2020 was a year of agile and innovative 
product development. The Group’s key 
strength is to innovatively address market 
needs with our products. 

We were quick to respond to COVID-19, 
producing one of the first tests in January 
2020. We maintained this pace through the 
year and launched new assays and work-
flow solutions to build a comprehensive 
COVID-19 product portfolio. 

Our broad technology base covers both 
protein and molecular platforms and a 
range of testing settings: near-patient, 
hospital laboratory and high throughput 
(“HT”). Therefore, we can develop a range 
of PCR, ELISA and lateral flow antibody 
and antigen tests for near patient, 
central labs, HT settings that can run on 
many laboratory systems as well as our 
own q16/q32 rapid PCR systems. Our 
internal R&D is complemented by an 
expert business development function, 
which has developed a global network of 
innovate partners and has successfully in-
licensed antibody, antigen and work-flow 
solutions. 

Across the COVID-19 market, testing 
requirements are increasing in complexity. 
There is a regulatory requirement for 
multi-gene assays (2 and 3 gene assays) 
that exclude the (S and N) genes that are 
most prone to mutations and for suppliers 
to provide detailed bio-informatics 
surveillance. We are well positioned with 
an expert bio-informatics team and will 
continue to invest in this area especially 
as we develop our plans for the non-
COVID-19 products.

During the period, the Group developed 
a new patent strategy to protect our 
novel content with the filing of patents 
now being a routine part of the Group’s 
product development process, forming a 
key part of protecting future value within 
the business.

We have filed over 20 patents to protect 
our proprietary assays, the q16/q32 PCR 
systems and work-flow innovations. This 
culture and practice of developing novel 
and cutting-edge diagnostic technology 
underpins the Group’s continued growth 
and agility. As such, the R&D team has 
more than doubled in size and now 
includes a leading bio-informatics team 
and the Group’s clinical trial function 
that undertakes clinical trials in the UK, 
Europe, USA and Latin America. This 
clinical expertise is a key requirement 
of the new IVD-R regulation and, as 

such, the Group has built an industry-
leading team, which completed over 
a dozen product validations in 2020, 
including the successful TVG validation 
of PROmate®, the best-in-class direct 
to PCR COVID-19 assay and the recent 
launch of VariPLEX™, the first CE-IVD 
registered COVID-19 variant detection 
assay. The Group’s clinical expertise also 
includes over a dozen physicians, clinical 
and laboratory scientists that provide real-
time scientific advice. This, coupled to our 
leading bio-informatics and surveillance 
functionality, enables the Group to 
remain at the forefront of new diagnostic 
innovation. 

By combining a broad technology base 
with an agile and innovative product 
development and clinical trial functionality, 
the Group is well positioned to rapidly 
address new areas of unmet need 
with market-leading products. The 
R&D outlook for 2021 is strong, with a 
record-breaking number of new products 
in development that will continue to 
meet the rapidly changing COVID-19 
requirements and address the broader 
non-COVID-19 respiratory, transplant and 
infectious disease markets.

Graham Mullis
Chief Executive Officer

Section 172(1)  
Statement

The Directors acknowledge their duty under 
s172 of the Companies Act 2006 and 
consider that they have, both individually 
and together, acted in the way that, in good 
faith, would be most likely to promote the 
success of the Company for the benefit of 
its members as a whole. In doing so, they 
have had particular regard to: 

•  the likely consequences of any decision 

in the long term  
The Group’s long-term strategic 
objectives, including progress made 
during the year, and principal risks to 
these objectives, are set out in the 
Chief Executive Officer’s Report on 
pages 22 to 24, and in the Principal 
Risks and Risk Management section 
on pages 66 to 72 respectively.

•  the interests of the Company’s 

employees  
Our employees are fundamental to the 
Group achieving its long-term strategic 
objectives, and further disclosure on 
how we look after the interests of our 
employees is contained in Principle 3 of 
the Corporate Governance Statement 
on pages 47 to 48. 

•  the need to foster the Company’s 

business relationships with suppliers, 
customer and others  
A consideration of our relationship with 
wider stakeholders and their impact on 
our long-term strategic objectives is 
disclosed in Principles 2 and 3 of the 
Corporate Governance Statement on 
pages 47 and 48. 

•  the impact of the Company’s 

operations on the community and the 
environment  
The Group operates honestly and 
transparently. We consider the impact 
of our day-to-day operations on the 
community and the environment, and 
how this can be minimised, as more 
fully explained in Principle 3 of the 
Corporate Governance Statement on 
pages 47 and 48. Further disclosure 
on how we promote a corporate 
culture based on ethical values and 
behaviours is included in Principle 8 of 
the Corporate Governance Statement 
on pages 54 and 55. 

•  the desirability of the Company 
maintaining a reputation for high 
standards of business conduct  
Our intention is to behave in a 
responsible manner, operating within 
a high standard of business conduct 
and good corporate governance. This 
is explained more fully in our Corporate 
Governance Statement on pages 46 
to 56, and is also encapsulated in our 
risk management framework on pages 
66 to 72. 

•  the need to act fairly as between 

members of the Company  
Our intention is to behave responsibly 
towards our Shareholders and to treat 
them fairly and equally so that they 
may also benefit from the successful 
delivery of our strategic objectives.

24
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Review

2020 highlights

•  The business finished 2020 

debt free with a cash balance in 
excess of £90 million

•  All key territories saw year-on-
year growth, with UK market 
sales increasing to £219.4 
million in 2020 vs £2.1 million 
in 2019

•  Profit after tax of £132.4 million 
in 2020 vs a loss of £5.7 million 
in 2019

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It gives me great pleasure to present my first 
Financial Review for the Novacyt Group.

James McCarthy
Chief Financial Officer

The business finished 2020 
debt free with a cash balance 
in excess of £90 million. 
Financial performance 
Group revenue increased (20x) to £277.2 
million), compared to £11.5 million for 
the full year of 2019. This was driven 
by the continued successful global 
commercialisation of the Company’s 
COVID-19 product portfolio, underpinned 
by one of the world’s first approved 
polymerase chain reaction (“PCR”) tests 
for the virus. Primerdesign accounted for 
the major part of this growth achieving 
£272.8 million of revenue in 2020 
compared with £5.5 million in 2019.

All key territories saw year-on-year 
growth, with the UK market seeing 
sales increase to £219.4 million in 2020 
compared with £2.1 million in 2019, 
largely driven by contracts supporting the 
UK testing pandemic response. Sales to 
Europe (excluding the UK) were £32.0 
million in 2020 compared with £2.7 million 
in 2019, driven by increased distributor 
sales of our range of COVID-19 tests. 
Sales to the Americas were £10.3 million 
compared £2.3 million in 2019. 

Primerdesign sales grew by over 
4,800% to £272.8 million, and was 
principally responsible for the Group’s 
growth during 2020, due to the success 
of the COVID-19 product portfolio, 
following the launch of one of the 

world’s first approved polymerase chain 
reaction (“PCR”) tests in Q1 2020. All 
geographical regions have experienced 
significant growth during 2020, with 
the UK, Middle East, Germany and US 
accounting for the main revenue growth. 
Primerdesign has been at the forefront 
of the global response to COVID-19 
testing requirements, selling into over 
85 countries in 2020. There have been 
several product launches to address 
emerging market needs including multiple 
gene tests, test panels to help differentiate 
COVID-19 from common winter diseases 
and new reagents to aid PCR testing 
workflow for users.

Lab21 sales decreased by £0.8 million 
in 2020 to £5.2 million, compared with 
sales of £6.0 million in 2019. There is £1.9 
million of intercompany sales included 
in the £5.2 million of Lab21 Products 
segment sales that are eliminated at a 
Group level in the consolidated Group 
accounts. This intercompany revenue 
relates to services that Microgen 
Bioproducts provided to Primerdesign in 
its manufacturing of COVID-19 kits, rather 
than outsourcing the task to a third party 
and thus diluting the gross margin. The 
Lab21 Products business was severely 
impacted in 2020 by its core customers 
diverting testing from veterinary and food 
testing to COVID-19 testing. As a result of 
strong partnerships built over many years, 
a number of Lab21 Products distributors 

migrated to purchasing COVID-19 tests 
from Primerdesign and significant sales 
were generated from key Lab21 Products 
customers as a result.

IT-IS International sales for the period 
post acquisition, 15 October to 31 
December 2020, totalled £6.9 million. 
There is £5.8 million of intercompany 
sales included in the £6.9 million of 
IT-IS International segment sales that 
are eliminated at a Group level in the 
consolidated Group accounts.

Group gross profit increased to £211.5 
million in 2020 compared with £7.3 milion 
in 2019, giving a Group gross margin of 
76.3% in 2020 compared with 64.0% 
in 2019. This continues the trend of 
increased gross margin every year since 
2014, driven by Primerdesign increasing 
its share of Group revenue to 98% from 
48% in 2019, and Primerdesign delivering 
a gross margin of 77% in 2020 compared 
with 85% in 2019, demonstrating strong 
control of margins as the business is 
scaled. During H1, Novacyt identified that 
it had operational capacity constraints due 
to its facility footprint and thus, to quickly 
scale the business and meet increasing 
demands, elements of manufacturing 
were outsourced. This, however, did not 
have a detrimental impact on the gross 
margin of the Group.

Group operating costs increased year-on-
year by £28.2 million, to £35.4 million in 
2020 compared with £7.2 million in 2019. 
To support the growth in the business, 
significant investment has been made in 
the workforce and headcount increased 
from 110 at the end of December 2019 to 
237 at the end of December 2020.

The acquisition of the IT-IS International 
business in Q4 resulted in an additional 
£0.3 million of operating costs in Q4 
and the effect in 2021 will be bigger as 
the annualised impact is seen. The main 
driver for the year-on-year cost increase 
was the Long Term Incentive Plan (“LTIP”) 
that commenced in November 2017 and 
vested in November 2020, which was 
linked to the Company’s share price. 

As a result of the significant share price 
increase in 2020, driven by the financial 
performance of the business, the LTIP 
liability that crystallised in 2020 accounts 
for £19 million of the year-on-year cost 
increase.

The Group delivered an EBITDA of 
£176.1 million in 2020 compared with 
breakeven in 2019 (£0.2 million), driven 
by significantly increased sales. In 2019, 
the NOVAprep® business continued to be 
reported under IFRS 5 and is disclosed 
as discontinued operations in the income 
statement, which did not impact EBITDA.

2020 delivered recurring operating profit 
of £174.8 million verses a recurring 
operating loss of £1.1 million in 2019, 
delivering an improvement of over 
£175 million, driven by increased 
sales. Amortisation and depreciation 
remained flat year-on-year at £1.3 million 
in 2020, as the significant scale up in 
manufacturing has been largely supported 
by third party manufacturers rather than 
significant capital investments. 

Total depreciation charges of £0.6 million 
(2019: £0.6 million) and amortisation 
charges of £0.7 million (2019: £0.7 
million) for 2020 are consistent with 2019. 
The 2020 depreciation charge includes 
£0.3 million of IFRS 16 leasing costs, 
predominantly covering the rental fees for 
Novacyt premises.

The Group has moved from an operating 
loss in 2019 of £1.6 million to an 
operating profit of £167.4 million in 
2020 and is stated after non-recurring 
charges amounting to £7.4 million. The 
2020 charges comprise a £5.8 million 
impairment charge in relation to the 
goodwill associated with the Lab21 
Products business, a £1.1 million 
impairment charge in relation to intangible 
assets associated with the Omega 
Infectious Diseases business and other 
non-recurring costs totalling £0.5 million. 
The other non-recurring costs include 
acquisition related expenses, site closure 
costs and other miscellaneous costs. 

The Group generated a total net profit 
of £132.4 million in 2020, compared 
with a net loss in 2019 of £5.7 million, 
and is stated after £1.6 million of gross 
borrowing costs (2019: £1.0 million), other 
financial expenses of £0.7 million (2019: 
£0.9 million) and tax of £32.7 million 
(2019: £nil) based on the increased profit 
generated by the Group in the year.

2020 saw a profit per share being 
generated of £1.94 vs a loss per share in 
2019 of £0.13, as a result of the Group 
delivering a total net profit for the year 
compared with a loss in 2019.

Post balance sheet event 
/ DHSC Dispute
On 9 April 2021, Novacyt announced it 
was in dispute with the DHSC in relation 
to its second supply contract and made 
a further update on 21 May 2021. The 
dispute primarily relates to Q4 2020 
revenue totalling £129.1m in respect of a 
specific product supplied to the NHS. The 
Company has taken independent legal 
advice and a provision has been made in 
the financial statements with the Board’s 
estimate at this time in respect of this 
claim with DHSC. 

The Board has formed a judgment that, 
in accordance with the contractual terms, 
and if required, it should be possible 
to replace the product in dispute and 
a product warranty provision has been 
made accordingly. The Board’s best 
estimate of the cost to replace is up to a 
maximum of £19.8 million, the timing of 
any outflow is dependent on settlement of 
the dispute. If no settlement is achieved 
and legal action is required, the timing of 
any possible outflow will be extended.

It is possible, but not probable, that 
the DHSC’s claim for a refund under 
the limited assurance warranty will be 
successful. The timing of any cash 
outflow is dependent upon the success 
of the claim and the terms negotiated for 
repayment. If the resolution of the claim 
is materially different from the Board’s 
determination of replacing the product, 

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Review

continued

the financial statements with regard to 
revenue and the provision for product 
warranty could be significantly impacted.

Of the Q4 2020 revenue, invoices 
amounting to £24.0 million in respect of 
product delivered to the DHSC remain 
outstanding at the date of signing the 
financial statements and recovery of this 
amount is also dependent on the outcome 
of the dispute. In addition, after the year-
end, a further £49.0 million of product 
delivered and invoiced to the DHSC in 
2021 remains unpaid and is now also part 
of the dispute. The unpaid invoices total 
£73.0 million and include VAT. 

Balance sheet
Goodwill has increased to £17.9 million 
in 2020 from £13.6 million in the previous 
year. Goodwill totalling £9.4 million was 
recognised on the acquisition of IT-IS 
International. This has been partially 
offset by a reduction in Lab21 Products 
goodwill following the annual impairment 
process, where an impairment charge of 
£5.8 million has been recorded, reflecting 
a prudent view of the future expected 
discounted cash flows generated from 
the business. The remaining £0.7 million 
goodwill increase is due to exchange 
differences on balances based in Euros.

A deferred tax asset of £3.0 million has 
been recorded in 2020, compared with 
a £nil prior year balance. £2.1 million of 
the balance relates to the portion of the 
LTIP charge that is recognised by Novacyt 
in the UK books, but will be deducted 
for taxation when payments are made in 
2021 and 2022. The remaining balance of 
£0.9 million arises from the elimination of 
the internal margin on products acquired 
by Primerdesign from Microgen and IT-IS 
International, and still held in stock at the 
year end.

Other non-current assets have increased to 
£6.1 million from £4.9 million in 2019. Other 
intangibles have increased by a net £0.6 
million, but includes additions totalling £2.6 
million, predominantly relating to the assets 
created as part of the IT-IS International 

28
28

acquisition (customer relationships and 
brands) offset by disposals (impairment of 
the Omega ID business intangible assets) 
and amortisation totalling a combined £2 
million. Property, plant and equipment has 
increased by a net £0.8 million, and includes 
£1.2 million of capital expenditure offset by 
charges (mainly depreciation) totalling £0.4 
million. The remaining £0.2 million decrease 
relates to the reduction in other long-term 
assets and financial assets.

Inventory increased in the year by £27.8 
million (1,335%) to £29.9 million to 
support the Group’s revenue growth, with 
significant finished goods being held in 
stock ready for immediate dispatch. As 
the lead time for obtaining some key raw 
materials is significant, bulk orders were 
placed to ensure there were no supply 
shortages, which also contributed to the 
higher inventory balance in 2020.

Trade and other receivables have 
increased in the year by £77.7 million 
(4,200%) to £79.6 million. Novacyt 
finished the year with strong sales in 
Q4 and this balance is reflective of that 
trading, with most of the balance being 
less than 30 days old. An expected credit 
loss provision of only £0.2 million was 
booked at year end, demonstrating a 
strong credit control process.

Other current assets have increased to 
£3.7 million in 2020 from £0.4 million in 
2019, driven by a £3.3 million increase 
in prepayments. The key balances at 31 
December 2020 include prepayments 
for annual Group commercial insurance, 
stock that was not delivered to 
Primerdesign in 2020, rent, rates and 
support costs.

All outstanding debt as at 31 December 
2019, totalling £7.1 million, was fully 
repaid during 2020 using cash generated 
in the year. The Group is now debt free 
and the closing 2020 balance is £nil.

The contingent consideration balance 
increased from £nil in 2019 to £1.8 
million in 2020 as a result of the two 
earnout milestones associated with the 
IT-IS International acquisition. It will be 
settled in two payment tranches, due in 
September 2021 and 2022, upon the 
achievement of certain deliverables.

Short-term provisions increased to £19.9 
million in 2020 from £0.04 million in 2019. 
A product warranty provision for £19.8 
million has been booked in 2020 to cover 
management’s view of the maximum 
cost of replacing products after receiving 
notification of a product warranty claim.

Trade and other liabilities increased to 
£36.8 million in 2020 from £3.9 million 
in 2019. Trade payables and accrued 
invoices have increased by £10.7 million 
in line with increased trading activity. In 
addition, the improved Group liquidity 
position has meant that credit facilities 
have been secured with many suppliers 
who previously did not offer such terms. 
The closing year end Value Added Tax 
(“VAT”) liability payable to HMRC in the 
UK, covering the months of November 
and December, has increased by £16.7 
million from 2019. The other key increase 
for £5.6 million is for the second tranche 
of the LTIP payment that is due to be paid 
in November 2021.

Corporation tax due at the end of 2020 
totalled £15.1 million from £nil in 2019, 
which reflects the UK corporation 
tax liability of the Group. The amount 
represents the tax due at the full UK rate 
(19%) on taxable profits, although in due 
course, if patents are granted and a Patent 
Box claim is made, future taxable profits 
should be taxable at a much lower rate.

Other long-term liabilities relates to the 
third tranche of the LTIP payment that is 
due to be paid in November 2022. The 
closing 2020 balance was £5.6 million, 
from £nil in 2019.

Cash flow
Cash has increased to £91.8 million 
in the year from £1.5 million in 2019, 
driven by the strong trading performance 
of the business. Net cash generated 
from operating activities increased to 
£103.0 million in 2020 driven by the 
EBITDA profitability of the business of 
£176.1 million offset by working capital 
expenditure of £73.2 million.

Net cash outflow from investing activities 
increased to £8.0 million in 2020 from 
£1.0 million in 2019. £6.9 million of the 
2020 balance is due to the net cash 
consideration paid for IT-IS International, 
where the cash paid in 2020 totalled 
£11.6 million less the £4.7 million cash 
acquired. Capital expenditure increased 
year-on-year to £1.1 million in 2020, to 
support the growth in the business, this 
being less than 1% of revenue.

Net cash outflow from financing activities 
in 2020 totalled £5.0 million vs a net 
inflow in 2019 of £2.5 million. The 2020 
cash outflow was primarily due to Novacyt 
paying down all outstanding debt as at 
31 December 2019. Debt repayments 
covering capital and interest, totalled £6.2 
million, a short-term financing facility was 
repaid in full totalling £0.7 million, lease 
payments of £0.3 million were made and 
these outflows were offset by a net cash 
inflow from the conversion of warrants 
totalling £2.2 million.

James McCarthy
Chief Financial Officer

Group revenue £’000

£277,204

for 2020
(2019: £11,468)

Group gross margin £’000

£211,500

for 2020
(2019: £7,340)

Group EBITDA £’000

£176,145

for 2020
(2019: £174)

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As Novacyt has grown, we 
have also increased our focus 
on Environment, Social and 
Governance (“ESG”) matters. 
We are pleased to share 
initial ESG data in this Annual 
Report and will continue to 
develop our approach over 
time. Environment and Social 
information is covered in this 
section, while our overall 
approach to Governance  
is addressed on page 46.

Environment: Measuring  
our impact

Streamlined Energy & Carbon Reporting
The section across includes Novacyt’s first year of reporting 
under the new Streamlined Energy & Carbon Reporting 
requirements.  
The reporting period is the same as the Company’s financial year, 
1 January 2020 to 31 December 2020.

Organisation boundary and scope of 
emissions
We have reported on all of the emission sources required under 
the Companies Act 2006 (Strategic Report and Directors’ 
Reports) Regulations 2018. These sources fall within Novacyt’s 
consolidated financial statement.

An operational control approach has been used in order 
to define the organisational boundary. This is the basis for 
determining the Scope 1, 2 and 3 emissions for which Novacyt 
is responsible, and includes emissions from Novacyt’s two 
operational facilities:

•  In October 2020, Novacyt acquired IT-IS International, 
manufacturer of its q16 and q32 instruments. For the 
purpose of this year’s baseline, we have excluded IT-IS 
from the organisational boundary for the year ending 31 
December 2020. The IT-IS acquisition will be adequately 
reflected in the subsequent reporting cycle for the year 
ending 31 December 2021;

•  We have included Microgen Bioproducts Ltd and Lab 21 
Healthcare Ltd (“Microgen”), based in Camberley, UK; and

•  Primerdesign, based in Southampton, UK.

The emissions sources that constitute the Company’s 
operational boundary for the year ending in 31 December 2020 
include:

Scope 1

Scope 1: energy use and related 
emissions from Novacyt’s fuel 
combustion (gas) and operation  
of facilities; 

Scope 2

Scope 2: energy use and 
related emissions from electricity 
purchased for Novacyt’s own use; 
and

Scope 3

Scope 3: energy use and related 
emissions from business travel in 
rental cars or employee-owned 
vehicles where Novacyt  
is responsible for purchasing  
the fuel.

Methodology
For reporting purposes, Novacyt has employed the services of a specialist advisor,  
to quantify and verify the Greenhouse Gas (“GHG”) emissions associated with Novacyt’s 
operations.

The following methodology was applied in the preparation and presentation of this data:

•  the Greenhouse Gas Protocol published by the World Business Council for 

Sustainable Development and the World Resources Institute (the “WBCSD/WRI GHG 
Protocol”); 

•  application of appropriate emission factors to Novacyt’s activities to calculate GHG 

emissions; 

•  Scope 2 reporting methods – application of location-based emission factors for 

electricity supplies;

•  inclusion of all the applicable Kyoto gases, expressed in carbon dioxide equivalents, 

or CO2e; and

•  presentation of gross emissions as Novacyt does not purchase carbon credits (or 

equivalents).

Total energy use
The total energy use for Novacyt for in the year ending 31 December 2020 was  
582,158 kWh. 

This represents a 70% increase in total energy use compared to the year ending 31 
December 2019 (343,325 kWh). The increase in total energy use in 2020 relative to 
2019 can largely be attributed to the significant scale-up of operations and production in 
response to the COVID-19 pandemic.

20194

Primer-
design

Microgen
Lab21

Microgen
Lab21

Total

2020

Primer-
design

Total

Gas 

13,530

32,226

45,756

18,653

42,144

60,797

Electricity 

230,060

67,510

297,569

296,498

224,863

521,361

Transport 

–

–

–

–

–

–

Total

243,590

99,736

343,325

315,151

267,007

582,158

Absolute emissions
The total Scope 1, 2 and 3 GHG emissions from Novacyt’s operations in the year ending 
31 December 2020 were 132.73 tonnes of CO2 equivalent (tCO2e), using a ‘location-
based’ emission factor methodology for Scope 2 emissions. 

This represents a 57% increase in total emissions compared to the year ending 31 
December 2019 (84.5 tCO2e). As with total energy use, the increase in total emissions in 
2020 relative to 2019 can largely be attributed to the significant scale-up of operations 
and production in response to the COVID-19 pandemic.

References: 

1  Scope 1 covers direct emissions from 

sources owned or controlled by the Company, 
including emissions from fuel combustion 
(e.g. emissions from combustion in owned 
or controlled boilers, furnaces, vehicles, 
etc.), process emissions (e.g. emissions from 
chemical production in owned or controlled 
process equipment), and fugitive emissions 
(e.g. intentional and unintentional). Of the 
aforementioned facilities or assets, only 
natural gas combustion within boilers is 
applicable to Novacyt’s operations. 

2  Scope 3 is an optional reporting category 

under the Greenhouse Gas Protocol. 
For emissions disclosure purposes, the 
operational boundary for Scope 3 emissions 
has been defined in accordance with 
UK SECR guidelines, in compliance with 
legal emissions disclosure responsibilities 
under the Companies and Limited Liability 
Partnerships Regulations 2018.

3  All emission factors sourced from the UK 
Government conversion factors for company 
reporting of greenhouse gas emissions for 
the years 2019 and 2020. 

4  The Company has used estimates in some 
instances to establish 2019 baseline.

5  Data obtained from fuel consumption (gas) 
bills for each of Novacyt’s two sites for the 
years 2019 and 2020, expressed in kWh.

6  Data obtained from direct electricity 

consumption bills for each of Novacyt’s two 
sites for the years 2019 and 2020, expressed 
in kWh.

7  Data obtained from business travel in rental 
cars or employee-owned vehicles where 
Novacyt is responsible for purchasing 
the fuel. Novacyt does not purchase fuel 
for business travel or employee-owned 
vehicles, as such transport emissions 
are not applicable based on the defined 
organisational boundary. 

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Novacyt Group Annual Report and Accounts for the year ended 31 December 2020

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continued

COVID-19 impact
The COVID-19 pandemic has had a substantial impact on Novacyt’s year-end 
performance due to the increased sales of the Company’s market-leading polymerase 
chain reaction (“PCR”) COVID-19 test. The volume of orders for the Company’s 
COVID-19 product portfolio and the Company’s new strategy implemented to continue 
growth trajectory, and consolidate performance through broadening focus on respiratory 
and transplant clinical diagnostics has been transformational for Novacyt, delivering 
sales growth of more than 2,300%. To meet the unprecedented demand for the 
Company’s PCR test following its launch, Novacyt initiated a programme to significantly 
scale-up the organisation. This included increasing the Company’s production capacity 
at the Primerdesign site in Southampton, UK. The increase in total emissions in 2020 
relative to 2019 can largely be attributed to the significant scale-up of the organisation to 
support laboratories and clinicians in the fight against the spread of COVID-19.

Figure 1.2 Absolute emissions (tCO2e)

2019

Primer-
design

5.9

17.3

–

Microgen
Lab21

2.5

58.8

–

Microgen
Lab21

3.4

69.1

–

Total

8.4

76.1

–

2020

Primer-
design

7.7

52.4

–

Total

11.2

121.6

–

61.3

23.2

84.5

72.6

60.2

132.8

Scope 18

Scope 29

Scope 310

Total

Figure 1.1 Breakdown of emissions by scope (tCO2e)

140.0

120.0

100.0

80.0

60.0

40.0

20.0

0.0

8.4

76.1

19

Scope 1

Scope 2
Scope 3

11.2

121.6

20

References: 

8  Scope 1 data calculated by multiplying total fuel consumption (gas – kWh) by the UK Government GHG 
Conversion Factor for natural gas (kWh [Gross CV]) defined for the given year (2019: 0.18385 kg  
CO2e/kWh; 2020: 0.18387 kg CO2e/kWh). 
9  Scope 2 data calculated by multiplying total electricity consumption (kWh) by the UK Government GHG 
Conversion Factor for electricity generated defined for the given year (2019: 0.2556 kg CO2e/kWh; 2020: 
0.23314 kg CO2e/kWh).
10  Novacyt does not purchase fuel for business travel or employee-owned vehicles, as such Scope 3 

emissions are not applicable based on the defined organisational boundary. 

Business 
Overview

Strategic 
Report

Our 
Governance

Financial 
Statements

Company 
Information

Intensity ratios
As well as reporting the absolute emissions, Novacyt’s GHG emissions are reported 
below on the metrics of kg of CO2 equivalent per full-time employee (“FTE”) and kg of 
CO2 equivalent per square foot of the occupied areas. These are the most appropriate 
metrics given that the majority of emissions result from the operation of Novacyt’s offices 
and the day-to-day activities of the employees. All of the intensity ratios have been 
calculated using Scope 1 and Scope 2 emissions only.

The intensity metrics based on floor area in the year ending 31 December 2020 was 
45.4 kg CO2e per m2. The employee number metric in the year ending 31 December 
2020 was 961.8 kg CO2e per FTE using the location-based method. 

Table 1.3 Intensity ratios

2019

2020

kg CO2e/FTE12

kg CO2e/m2 13 

kg CO2e/FTE 

kg CO2e/m2 15 

Scope 1

Scope 2

Scope 3

Total GHG 
emissions

73.8

667.2

–

741.0

2.9

26.0

–

28.9

81.0

880.8

–

961.8

3.8

41.6

–

45.4

Energy efficiency actions undertaken
Novacyt has taken a number of actions to increase the business’s energy efficiency in 
the year ending 31 December 2020, focused on: 

i.  Reducing absolute energy consumption through capital investment projects; and

ii.  Reducing energy consumption per unit output through scaling up production 
(economies of scale), increasing asset utilisation, and increasing automation.

Principal actions reported have had a direct impact on the energy efficiency related to 
Scope 1 and Scope 2 emissions, as defined by the Company’s operational boundary 
for the year ending in 31 December 2020. For increased transparency in emissions 
disclosure reporting, additional information has been provided on actions impacting the 
energy efficiency related to Scope 3 emissions despite falling outside the Company’s 
operational boundary. 

References: 

11 Number of FTE equivalents calculated based on total headcount from Novacyt operations, adjusted to 

remove discontinued operations (2019) and the IT-IS International Ltd acquisition made in October 2020. 

12  Number of FTE equivalents in 2019 was 114.

13  Number of FTE equivalents in 2020 was 138. FTE increase can be attributed to the significant scale-up of 
the organisation during the COVID-19 pandemic, including the addition of a number of new hires across 
operations.

14  Building area in 2019 was 2,923 m2.

15  Building area in 2020 was 2,923 m2.

32
32

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continued

Details of relevant energy efficiency actions can be found in Table 1.4 below. Resulting energy savings from the actions listed have not 
been quantified. 

Table 1.4 Energy efficiency actions

Principal actions  
(Scope 1 and Scope 2)

Energy efficiency action
Reduced energy 
consumption (absolute)
•  Capital investment projects 
Novacyt has invested in new 
equipment to reduce energy 
consumption, including new heat 
sealers in kitting and LED light 
fittings with light sensors at the 
Company’s two operational facilities 
(Microgen/Lab21 and Primerdesign).

Additional information 
(Scope 3)

Energy efficiency action
Reduced transportation 
across the value chain
•  Reduced global transportation 
RNase-free water production has 
been brought in-house, displacing 
the need for RNase-free water 
procurement from North America.

•  Reduced road transportation 

Newly localised manufacturing and 
storage has reduced the need for 
movement between sites.

Energy efficiency action
Reduced energy 
consumption (per unit 
output)
•  Improved energy efficiency 

through economies of scale  
Novacyt has increased 
manufacturing capacity to meet 
demand without expanding the 
Company’s real estate footprint, 
leading to increased output relative 
to overhead energy consumption.

•  Increased asset utilisation 
Novacyt has improved asset 
utilisation efficiency by optimising 
manufacturing batch size, adopting 
more efficient practices, and scaling 
up asset size commensurate with 
the ramp up in operations.

•  Increased automation  

Dispensing methods were moved 
from manual methods to automated 
methods to increase labour 
efficiency. 

Managing waste 
Novacyt’s manufacturing process generates very low levels of non-hazardous and 
hazardous waste. This is an area of the manufacturing operations that will receive more 
focus in 2021 as we introduce more rigorous measurement and a more comprehensive 
set of waste reduction measures. 

Business 
Overview

Strategic 
Report

Our 
Governance

Financial 
Statements

Company 
Information

Reducing packaging 
•  Improved packaging 

New packaging features more 
sustainable materials. This 
includes a change from foil 
pouches and foam inserts to 
recyclable lightweight card and 
plastic bags with direct printing  
in place of standard labels. 

•  Improved product design 

New PROmate® design features 
less plasticware, pipettes, PPE, 
and laboratory decontamination 
materials to reduce end-to-end 
consumables. New laser-etched 
barcodes have replaced standard 
labels to reduce material usage. 

•  Reduced waste 

Novacyt has taken action 
to reduce single-use waste 
by increasing the materials 
reused and recycled through 
the Company’s operation. 
This includes an updated anti-
contamination procedure to 
move from single-use disposable 
lab coats to reusable lab coats, 
and implementation of a standard 
recycling practice across all sites 
using recycling bins, compactors, 
and third-party recycling 
organisations. 

•  Improved product design 

The exsig® direct to PCR and 
PROmate® product streamline 
process for the end user and 
reduce the need for downstream 
energy intensive processing 
stages.

Social: supporting our 
people and wider society
At Novacyt, we take pride in how our work 
positively impacts people’s global health, 
most recently with our products in the front 
line of the fight against COVID-19. Our 
employees are at the heart of what we do, 
and their hard work and dedication were 
critical to our success in 2020. We also 
actively look for ways to support wider 
society.

Employees 
Diversity and inclusion 
Novacyt actively supports diversity and 
inclusion, and seeks to create a culture 
where everyone feels comfortable to 
be themselves at work and have their 
contribution valued, and where individual 
differences can be celebrated. This 
approach is captured in our Equality, 
Inclusion and Diversity policy.

In 2020, Novacyt’s workforce was 52% 
female, and 53% of managers were 
women. There are five Non-Executive Board 
members: one white female and four  
white males.

Pay gap analysis
Novacyt’s Company headcount in 2020 
was fewer than 250, and so was below the 
threshold to conduct pay gap analysis; this 
will be reviewed as the Company continues 
to evolve.

Health and safety
At Novacyt, we have a clear policy on health 
and safety. Employees are provided with 
health and safety training, and protective 
clothing and other equipment if required. 
Novacyt complies with the OHSAS 18001 
standard.

In 2020, no injuries were reported at work. 

Employee turnover and growth
Novacyt’s workforce expanded in 2020 due 
to the rapid growth of the business. The 
number of full-time equivalents rose from 
110 in 2019 to 237 in 2020. The unplanned 
turnover rate was 11%.

Whistleblower protection 
Novacyt complies with the Employment 
Rights Act 1996, which provides protection 
for workers who ‘blow the whistle’ in 
the public interest and has a policy for 
employees to follow. 

Anti-bribery
Integrity and transparency are of the utmost 
importance to Novacyt and we expect 
everyone connected with our business to 
comply with the highest ethical standards. 
We have a zero-tolerance approach to bribery 
and corrupt activities of any kind, whether 
committed by employees or by third parties 
acting for or on behalf of the Company. 

Training
We have launched a management 
development programme for all employees 
with people management responsibility. 
We have also launched a sales training 
programme for all sales employees. 
In addition to these group training 
programmes, individuals are supported 
with ad hoc training courses as and 
when required, to enable them to fulfil 
their role, e.g. bio-safety training, and we 
support employees who wish to undertake 
professional qualifications.

Supporting communities and 
wider society 
Charitable giving
At Novacyt, we believe in contributing to 
communities where we operate, and we 
have made donations to various charities 
and schools in the Camberley, Southampton 
and Middlesborough areas. As a result of the 
Company’s growth in 2020, a fund has been 
established to support a range of charitable 
initiatives. 

To support efforts to tackle the COVID-19 
pandemic in Africa, Novacyt is working 
in partnership with non-governmental 
organisations such as Unicef and the 
World Health Organization to provide tests. 
Primerdesign signed a 12-month long-term 
agreement with UNICEF in July 2020 and 
supplied COVID-19 qPCR testing kits to 
Nigeria, Tunisia and Palestine throughout the 
financial year. 

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Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020An 
internationally  
diversified 
Board 

The Directors present their Report together 
with the audited financial statements for the 
year ended 31 December 2020. The Corporate 
Governance Statement on pages 46 to 56 also 
form part of the Directors’ Report.

It is my pleasure to present our  
Corporate Governance Statement for  
the year ended 31 December 2020.

James Wakefield
Chairman

G
O
V
E
R
N
A
N
C
E

36

3737

The Board of  
Directors

James Wakefield
Non-Executive Director and Chairman of the Board
James is an experienced private equity investor, having spent over 30 years in the 
finance industry. He has been involved with over 50 businesses of varying sizes and 
stages of development across a wide range of sectors, including board representation 
as chairman or non-executive director in a number of these. He is chairman of 
WestBridge Capital LLP of which he was a founder partner in 2008. He previously spent 
18 years at Bridgepoint (previously NatWest Equity Partners) and, prior to that, spent 
four years at NatWest Markets/NatWest Investment Bank. He is also Chairman of the 
Nomination Committee and a graduate of Harvard Business School (AMP).

Graham Mullis
Chief Executive Officer
Graham was appointed Chief Executive Officer of Novacyt in 2014, having previously 
been Chief Executive Officer of Lab21 since 2008. He has over 30 years of 
experience in the diagnostics, pharmaceuticals and medical device markets. Over 
the years, he has led and been involved in multiple successful exits, including that 
of Biocompatibles Eyecare, ClearLab International, VisionTec and Lab21. He also 
founded a pharmaceutical licensing company, Optivue, which focuses on repurposed 
drugs. Previous roles have included acting as a C-level executive with Biocompatibles 
International plc, a FTSE 250 company, and 1-800 CONTACTS, a NASDAQ-listed 
company.

He holds degrees in BSc Biochemistry and Physiology from Southampton University, 
UK, and an MBA in Business Administration from Warwick Business School, UK.

James McCarthy
Chief Financial Officer
James joined the Group as Chief Financial Officer in January 2021. He has over 30 
years of finance experience in international businesses in both consumer and B2B 
and in both private equity and publicly listed companies. During his career, he has led 
large-scale transformation initiatives both organic and supported by M&A. He has also 
held general management roles, which gives him broad commercial experience and a 
strong appreciation for effective business partnership. He is a Fellow of the Association 
of Chartered Certified Accountants. James was appointed Chief Financial Officer of 
Novacyt in January 2021 and will be proposed for election as a Director of the Company 
at the next AGM, due to be held in September 2021 when he will replace Anthony Dyer 
on the Board.

Anthony Dyer
Chief Corporate Development Officer
Anthony joined the Group in 2010, and was Chief Financial Officer from January 
2017–2021, before taking on a new role as Chief Corporate Development Officer at the 
beginning of 2021. He has over 20 years of experience in healthcare, pharmaceuticals 
and medical devices, working primarily with growth companies and executing capital 
raising and M&A. Transactions executed include Novacyt’s acquisitions of Primerdesign 
and IT-IS International, and BioFocus’ combination with Galapagos and Galapagos’ 
€130 million divestment of its service division to Charles River Laboratories.

He holds a BSc (Hons) degree in Maths and Management Science from University of 
East Anglia, UK. He is a Fellow of the Association of Chartered Certified Accountants.

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Directors 

continued

Juliet Thompson 
Independent Non-Executive Director
Juliet has 20 years of experience working as an investment banker and strategic advisor 
to healthcare companies in Europe. She has built a strong track record of advising 
companies on corporate strategy, equity and debt fundraisings and international M&A. 
Her experience includes senior roles (managing director, head of corporate finance and 
partner) at Stifel Financial Corp, Nomura Code Securities and WestLB Panmure. Juliet 
sits on the board of Vectura, an industry-leading device and formulation business for 
inhaled products, Indivior PLC, a U.K. listed global pharmaceutical company working 
to develop medicines to treat addiction and Organox Ltd, a private company that was 
spun out of Oxford University. 

Juliet is also a trustee of Leadership through Sport & Business, a social mobility-
focused charity, and trustee of the De Hann family trusts and director of their associated 
investment companies.

She is a member of the Institute of Chartered Accountants in England and Wales (ACA) 
and holds a BSc degree in Economics from the University of Bristol, UK.

Juliet is Chair of the Audit Committee and is a member of the Remuneration and 
Nomination Committee.

Andrew Heath MD, PhD
Independent Senior Non-Executive Director
Andrew is a healthcare and biopharmaceutical Executive with in-depth knowledge of 
the US and UK capital markets, with international experience in marketing, sales, R&D 
and business development. In addition to his role as Senior Independent Director for 
Novacyt since 2015, he is also currently chairman of TauC3 Biologics Ltd. He served as 
Chairman of Shield Therapeutics plc from 2016-2018 and as a non-executive director of 
Oxford Biomedica plc from 2010-2021.

From 1999–2008, Andrew was the chief executive officer of Protherics plc, taking the 
company from 30 to 350 members of staff and managing its eventual acquisition by 
BTG plc for £220 million. Prior to this, he served as vice president of marketing and 
sales for Astra Inc in the US, and worked within clinical and academic medicine at 
Vanderbilt University. He is also a former director of The BioIndustry Association.

He graduated in medicine from University of Gothenburg, Sweden, where he also 
completed his doctoral thesis in human toxicology. He is a fellow of the American 
Academy of Clinical Toxicology and a fellow of the UK Institute of Directors.

Andrew is Chairman of the Remuneration Committee, and a member of the Audit  
and Nomination Committees. 

Edwin Snape, PhD
Independent Non-Executive Director
Ed has over 40 years of experience in founding, investing in and guiding the 
development of many public and private healthcare and specialty materials companies. 
He was a founder of NMT Capital (a successor of Nexus) and continues to serve as 
one of its senior advisors. He is also a senior advisor to Maruho Co., Ltd. Prior to NMT 
Capital, Ed was managing general partner of The Vista Group, at the time a leading east 
coast venture capital firm; chairman of Orien Ventures, a private equity firm with Pacific 
Rim affiliations, and a director of the Cygnus Funds, two UK-based private equity firms 
that specialised in investments throughout Europe. He was also a founder of Indonesia 
Growth Fund, a private equity fund based in Indonesia. Early in his career, he founded 
the Liposome Company, which listed and was later sold to Elan Corporation. Over 
the years, he has been a recipient of several awards in the material sciences industry, 
including the AB Campbell Award and the Hunt Silver Medal. He also holds several 
patents in the advanced materials field where he has pioneered various technological 
innovations and authored numerous technical papers.

He holds BSc and PhD degrees in Metallurgy from Leeds University, UK. Ed is a 
member of the Remuneration Committee.

Jean-Pierre Crinelli
Independent Non-Executive Director
Jean-Pierre is one of Novacyt’s founders, having established the business in July 2006. 
He has some 30 years of experience in the car and electrical components industry, with 
various roles in M&A and business restructuring. During this period, he was located for 
ten years in Singapore, North America, Belgium and Italy.

He holds a Diplôme from ESC Le Havre (business school, France) and a DECS (Diplôme 
d’Etudes Comptable Supérieures, national diploma).

Jean-Pierre is a member of the Audit Committee.

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team

Directors’  
Report

General information  
and principal activity
Novacyt S.A. is a public limited company 
incorporated and registered in France with 
registered number 491 062 527.

Results and dividend
The results for the period and financial 
position of the Company and the Group 
are as shown in the financial statements 
and are reviewed in the Strategic Report.

Review of business
The Chairman’s Statement on page 12, 
the Chief Executive Officer’s Report on 
page 22 and the Strategic Report on 
pages 12 to 35, provide a review of the 
business, the Group’s trading for the 
year ended 31 December 2020, key 
performance indicators and an indication 
of future developments and risks, and 
form part of this Directors’ Report.

The Company is listed on both Euronext 
Growth Paris and on the Alternative 
Investment Market (“AIM”) of the London 
Stock Exchange. Its principal activities in 
the year under review were specialising in 
infectious disease diagnostics.

Future developments
Likely future developments in the business 
of the Group are discussed in the 
Strategic Report.

Since its inception, the Company has 
not paid any dividends and the Directors 
do not intend to recommend a dividend 
at present. In the future, the Company’s 
dividend policy will form part of a wider 
review of capital allocation, which will 
be formulated in conjunction with the 
requirements of the business.

The Directors will only recommend 
dividends when appropriate, and they 
may, from time to time, revise the 
Company’s dividend policy. No dividends 
will be proposed for the financial year 
ended 31 December 2020 so we can 
invest in R&D, manufacturing and 
commercial aspects of the business.

Directors
The Directors of the Company who served 
during the year ended 31 December 
2020, and up to the date of this Report 
are listed below.

The brief biographical details of the 
currently serving Directors are set out on 
pages 36 to 41.

Director

Capacity

James Wakefield Non-Executive 

Director and Chairman 
of the Board

Graham Mullis 

Chief Executive Officer

Anthony Dyer 

Juliet Thompson 

Chief Corporate 
Development Officer

Independent Non-
Executive Director

Dr Andrew Heath  Independent Senior 

Dr Edwin Snape 

Non-Executive 
Director

Independent Non-
Executive Director

Jean-Pierre 
Crinelli

Independent Non-
Executive Director

James McCarthy, Chief Financial Officer, will be 
proposed for election as a Director of the Company 
at the next AGM due to be held in September 2021 
when he will replace Anthony Dyer on the Board.

Directors’ interests
The Directors’ interests in the Company’s 
shares and the Novacyt LTIP are shown 
in the Directors’ Remuneration Report on 
pages 58 to 61.

No Director has any beneficial interest 
in the share capital of any subsidiary or 
associate undertaking.

Graham Mullis 
Chief Executive 
Officer

James McCarthy
Chief Financial Officer

Anthony Dyer 
Chief Corporate 
Development Officer 

Paul Eros
Chief Business Officer

Trevor Reginald
Chief Technology 
Officer

Guillermo Raimondo
Chief Commercial 
Officer

David Franks
Chief Human 
Resources Officer

Nick Plummer
General Counsel and 
Company Secretary

Mandy Cowling
Corporate and 
Investor Relations 
Manager

Steve Gibson 
Group Finance 
Director

Lisa Henriet
Group Operations 
Director

Navin Nauth-Misir
QA/RA Director

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Report 

continued

Directors’ indemnity 
provisions
The Directors have the benefit of an 
indemnity, which is a qualifying third-party 
indemnity provision as defined by s236 of 
the Companies Act 2006. The indemnity 
was in force throughout the financial 
period and at the date of approval of 
the financial statements. In addition, the 
Group has purchased and maintains 
Directors’ and Officers’ liability insurance 
in respect of itself and its Directors.

Political and  
charitable donations
The Company made a number of small 
charitable donations during the reporting 
period, in addition to creating a charity 
committee responsible for organising 
larger charitable donations during 2021.

Financial instruments – 
risk management
The Group’s financial risk management 
policy is set out in note 44 to the financial 
statements.

Share capital structure
The Company’s share capital, traded 
on Euronext Growth Paris and AIM, 
comprises a single class of ordinary 
shares each having a nominal value of 
1/15th of one Euro. Except as otherwise 
provided by law, every Shareholder has 
one vote for every fully paid up share of 
which they are the holder. Each ordinary 
share creates a share in the Company’s 

44
44

assets, profits and in any liquidation 
surplus. In the event of a liquidation of 
the Company, any outstanding cash 
would be distributed to each Shareholder 
in proportion to their holdings in the 
Company.

The share rights follow the ordinary shares 
from owner to owner and any transfers 
of the shares include all dividends due 
and unpaid, and those due and, where 
applicable, the share of the reserves 
(following payment of any outstanding 
liabilities) of the Company.

Movements in the Company’s issued 
share capital during the year under review 
are set out in note 31 to the financial 
statements.

As of 31 December 2020, the Company’s 
share capital of €4,708,416.54 was 
divided into 70,626,248 shares with a par 
value of 1/15th of a Euro each. 

Major interests
As at 31 March 2021, the Company had 
been notified of the following significant 
shareholdings of approximately 3% and 
4% of the issued share capital of the 
Company: 

Number of 
shares held 

Percentage 
of issued 
shares 

2,952,681 

4% 

2,085,368

2.95% 

Shareholder 
Vatel Capital 
BlackRock 
Inc 

UK Bribery Act 2010
The Group is committed to complying 
with the UK Bribery Act 2010, both within 
its UK and overseas business activities.

As such, the Group has implemented 
an anti-bribery policy, which has been 
adopted by the Board, designed to 
ensure that the Group operates in an 
open, transparent and ethical manner. 
This policy applies to the Board 
and employees of the Group, and 
to temporary workers, consultants, 
contractors and agents acting for, or on 
behalf of, the Group (both in the UK and 
overseas). The policy generally sets out 
their responsibilities in observing and 
upholding a ‘zero tolerance’ position on 
bribery in all jurisdictions in which the 
Group operates, as well as providing 
guidance to those working within the 
Group on how to recognise and deal 
with bribery issues and the potential 
consequences.

Management at all levels of the Group 
is responsible for ensuring that those 
reporting to them, internally and externally, 
are made aware of and understand this 
policy.

Significant agreements
The Company is not party to any 
significant agreement that takes effect, 
alters or terminates upon a change of 
control of the Company other than the 
Directors’ service contracts, details of 
which are set out in the Remuneration 
Report.

Statement of engagement 
with suppliers, customers 
and others in a business 
relationship with the 
Group 
The Directors are mindful of their statutory 
duty to act in a way they each consider, 
in good faith, would be most likely to 
promote the success of the Group for 
the benefit of its members as a whole, as 
set out in the s172(1) statement on page 
25. A review of the Group’s approach to 
developing and maintaining relationships 
with its wider stakeholders, and the 
impact on the Group’s long-term strategic 
objectives, is set out under Principle 3 of 
the Corporate Governance Statement on 
pages 46 and 56.

Significant post-balance 
sheet events
On 9 April 2021, Novacyt announced it 
was in dispute with the DHSC in relation 
to its second supply contract and made 
a further update on 21 May 2021. The 
dispute primarily relates to Q4 2020 
revenue totalling £129.1m in respect of a 
specific product supplied to the NHS. The 
Company has taken independent legal 
advice and a provision has been made in 
the financial statements with the Board’s 
estimate at this time in respect of this 
claim with DHSC. 

Of the Q4 2020 revenue, invoices 
amounting to £24.0m in respect of 
product delivered to the DHSC remain 

outstanding at the date of signing the 
financial statements and recovery of 
this amount is also dependent on the 
outcome of the dispute. In addition, after 
the year-end, a further £49.0m of product 
delivered and invoiced to the DHSC in 
2021 remains unpaid and is now also part 
of the dispute. The unpaid invoices total 
£73.0m and include VAT. 

Going concern
The Directors have, at the time of 
approving the financial statements, a 
reasonable expectation that the Company 
has adequate resources to continue in 
operational existence for the foreseeable 
future. Thus, they adopt the going 
concern basis of accounting in preparing 
the financial statements.

The going concern model covers the 
period up to and including June 2022. 
In making this assessment, the Directors 
have considered the following elements: 

•  the working capital requirements of the 

business;

•  a positive cash balance at 31 

December 2020 of £91,765,000;

•  payment of the second tranche of the 
LTIP that commenced in November 
2017; 

•  payment of the first earn-out milestone 

related to the IT-IS International 
acquisition; and

•  Management’s confidence in settling 

The forecast prepared by the Company 
shows that it is able to cover its cash 
needs during the financial year 2021 and 
until June 2022 without the raising of any 
banking or other financing facility. 

Independent Auditor
Deloitte LLP has indicated that they are 
willing to continue in office as the Group’s 
Auditor.

Disclosure of information 
to the Auditor
As far as the Directors are aware, there 
is no relevant audit information (that 
is, information needed by the Group’s 
Auditor in connection with preparing their 
report) of which the Group’s Auditor is 
unaware, and each Director has taken 
all reasonable steps that they ought 
to have taken as a Director in order to 
make themself aware of any relevant 
audit information and to establish that 
the Group’s Auditor is aware of that 
information. 

Annual General Meeting
The Annual General Meeting of the 
Company will be held in September 2021, 
further information can be found on the 
companies website at www.novacyt.com.
By order of the Board

the outstanding commercial dispute as 
per note 50 in the Group accounts.

James McCarthy
Chief Financial Officer 

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from the Chairman

QCA  
principles

Dear Shareholders,
As Chairman of Novacyt S.A., it is 
my responsibility to lead the Board to 
ensure that the Group has in place the 
strategy, people, structure and culture to 
deliver value to Shareholders and other 
stakeholders of the Group over the medium 
to long term. Due to the massive growth 
and resulting changes that the Group 
experienced during 2020, we have had 
to make a number of changes to reflect 
the larger business we are today. This has 
included improving various processes/
systems and recruiting new staff members 
including strengthening and reshaping the 
Executive team and the Board. There are 
two matters to note relating to this:

•  Anthony Dyer has taken on the role 
of Chief Corporate Development 
Officer and James McCarthy has been 
recruited as Chief Financial Officer.  
Subject to Shareholder agreement at 
the AGM, James will join the Novacyt 
SA Board and Anthony will step down 
at that time. I would like to put on 
record my thanks to Anthony for all his 
hard work as CFO.

•  Good governance dictates that Non 

Executive Directors can only serve for 
a finite term and therefore during 2021 
we will need to find a replacement for 
Edwin Snape who has been involved 
with the company (in its various guises) 
for over 10 years. This will also ensure 
compliance with French regulation 
concerning the proportion of Directors 
over the age of 70. I would like to 
thank Ed for the contribution he has 
made and the support he has provided 
over the years.

A number of new internal control 
procedures and positive actions have 
been implemented and finalised, whilst 
other areas for improvement continue 
to be identified. On behalf of the Board, 
I am, therefore, pleased to present our 
Corporate Governance Statement for the 
year ended 31 December 2020.

Novacyt S.A. is incorporated in France 
and is listed on Euronext Growth Paris and 
AIM. The Directors recognise the value and 
importance of high standards of corporate 
governance. As the Company is traded on 
AIM, it is not required to comply with the 
UK Corporate Governance Code. However, 
the Board has adopted the 2018 Quoted 
Companies Alliance Corporate Governance 
Code (the “QCA Code”) as the basis of 
the Group’s governance framework. The 
Company complies with the provisions of 
the QCA Code as far as is practicable for a 
company of Novacyt S.A.’s size, nature and 
stage of development, and in accordance 
with the regulatory framework that applies 
to companies admitted to trading on AIM. 
The Company also continues to comply 
with all the requirements of being listed on 
Euronext Growth Paris.

It is the responsibility of the Board to 
ensure that the Group is managed for the 
long-term benefit of all Shareholders and 
stakeholders, with effective and efficient 
decision making. Corporate governance 
is an important aspect of this, reducing 
risk and adding value to our business. 
As individual Directors, we are mindful of 
our statutory duty to act in the way each 
of us considers, in good faith, would be 
most likely to promote the success of the 
Company for the benefit of its members 
as a whole, as set out in our s172(1) 
statement on page 25.

The QCA Code sets out ten principles, 
in three broad categories, and in this 
Corporate Governance Statement, I have 
set out the Group’s application of the 
QCA Code, including, where appropriate, 
cross references to other sections of the 
Annual Report and to our website. 

James Wakefield
Non-Executive Director and  
Chairman of the Board 

Deliver growth

1.  Establish a strategy 
and business model 
that promote long-term 
value for Shareholders 

The Board is responsible to Shareholders 
for setting the Group’s strategy by: 
maintaining the policy and decision 
making process around which the 
strategy is implemented; ensuring that 
necessary financial and human resources 
are in place to meet strategic aims; 
monitoring performance against key 
financial and non-financial indicators; 
providing leadership whilst maintaining 
the controls for managing risk; overseeing 
the system of risk management; and 
setting values and standards in corporate 
governance matters.

The Board has established a strategy and 
business model which seek to promote 
long-term value for Shareholders and the 
business is focused on three strategic 
pillars of growth:

•  Organic growth

•  Innovative R&D

•  Acquisition 

A fuller explanation of how the strategy 
and business model are executed is  
set out on pages 18 and 19 of the  
Strategic Report. 

2.  Seek to understand and 
meet Shareholder needs 
and expectations 

The Company has a strong commitment 
to market communication, with the 
Directors seeking to be accountable 
against the stated strategic objectives 
of the Group. The Company maintains 
regular contact with Shareholders through 
publications such as the Annual Report 

and Accounts, operational updates, 
regular press announcements made via 
a regulatory information service and the 
Company’s website. 

The Company is responsive to 
Shareholder telephone and email 
enquiries throughout the year and the 
Board regards the AGM as a particularly 
important opportunity for Shareholders 
and members of the Board to meet and 
exchange views.

The Company receives occasional 
feedback direct from investors, which is 
carefully considered by the Board, with 
appropriate action being taken where 
the Board believes it in the interests 
of Shareholders to do so. None of the 
feedback received from investors has 
involved non-compliance with the QCA 
Code.

3.  Take into account wider 
stakeholder and social 
responsibilities and their 
implications for long-
term success 

In addition to its Shareholders, the 
Company believes its main stakeholder 
groups are its employees, clients, 
suppliers and relevant statutory authorities 
in its areas of operation.

The Group is committed to maintaining 
the highest standards of corporate social 
responsibility in its business activities by: 
aiming to comply with all applicable laws 
and regulations, wherever the Group 
operates; achieve and comply with 
relevant quality and people management 
standards; consult with and respond to the 
concerns of its stakeholders; work towards 
realising the Group’s mission and vision 
statements; and behave with honesty and 
integrity in all the Group’s activities and 
relationships with others and reject bribery 
and corruption in all its forms.

The Board recognises the benefits of a 
diverse workforce, which enables the 
Group to make better decisions about 
how to optimise resources and work by 
eliminating structural and cultural barriers 
and bias. It allows us to: protect and 
enhance our reputation by recognising 
and respecting the needs and interests 
of diverse stakeholders: deliver strong 
performance and growth by attracting, 
engaging and retaining diverse talent; and 
innovate by drawing on the diversity of 
perspectives, skills, styles and experience 
of our employees and stakeholders. 

The Group is committed to ensuring that it 
treats its employees fairly and with dignity. 
This includes being free from any direct 
or indirect discrimination, harassment, 
bullying or other form of victimisation. The 
Group has policies in place to encourage 
employees to speak up about any 
inappropriate practices or behaviour.

It was important for us to look after our 
employees during 2020 as they are 
keyworkers and the majority had to come 
into work during lockdown. We continued 
to pay employees who had to shield, 
self-isolate or take time off for childcare. 
We also introduced a bonus to recognise 
that our employees were working 
particularly hard during these challenging 
times. At the end of 2020, we introduced 
a COVID-19 screening programme, 
using our tests, to prevent the spread 
of Coronavirus amongst the workforce. 
During this time, we reminded our 
employees of the Employee Assistance 
Programme, which provides 24/7 support 
for any issues they were facing during 
this time, particularly with mental health 
challenges, relationship issues, etc.

The Group believes that having 
empowered and responsible employees 
who display sound judgement and 
awareness of the consequences of their 
decisions or actions, and who act in an 
ethical and responsible way, is key to the 
success of the business. 

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James Wakefield
Non-Executive Director  
and Chairman of the Board

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principles  

continued

The operation of a profitable business 
is a priority and that means investing for 
growth as well as providing returns to its 
Shareholders. To achieve this, the Group 
recognises that it needs to operate in a 
sustainable manner and therefore has 
adopted core principles to its business 
operations, which provide a framework 
for both managing risk and maintaining 
its position as a good ‘corporate citizen’, 
and also to facilitate the setting of goals to 
achieve continuous improvement. 

The Group encourages feedback from its 
clients through engagement with individual 
customers. As a consequence of such 
feedback, the Group has collaborated with 
multiple existing and prospective clients to 
develop and validate new products, work 
flows and know-how to improve accuracy, 
reduce testing turnaround times, cost 
per test, and ultimately deliver improved 
clinical outcomes for millions of individual 
patients globally.

The Board is aware of the need to 
maintain good working relationships with 
the Group’s key suppliers and receives 
regular updates from the Executive team 
on key supply agreements. 

Health and safety
The Group is committed to complying 
with all relevant health and safety 
regulations to its operations. As such, 
the Group has adopted a Health & Safety 
Policy, which forms part of the Employee 
Handbook issued to all employees upon 
commencement of employment within the 
Group. The policy sets out arrangements 
and responsibilities across the Group and 
includes aspects such as: emergency 
procedures; security recommendations; 
accidents/incidences and first aid; manual 
handling/lifting and moving; work-related 
upper limbs disorders (including strains 
to hands and arms); display screen 
equipment/visual display equipment; 
alcohol and drugs policy; smoking policy; 
and COVID-19 in the workplace.

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The Group is not aware of any orders 
made in respect of a breach of health and 
safety regulation during the period.

Environment
The Directors consider that the nature of 
the Group’s activities is not detrimental to 
the environment. The Group continues to 
maintain the necessary levels of quality 
control and quality assurance through 
the application of its various quality 
management systems. Manufacturing 
facilities operate to the current revisions 
of ISO 13485:2016 and ISO 9001:2015 
as applicable.

4. Embed effective risk 
management, considering 
both opportunities and 
threats, throughout the 
organisation

The Board has overall responsibility for 
the Group’s system of internal control 
and for reviewing the effectiveness of 
internal control to safeguard Shareholders’ 
investment and the Group’s assets. There 
is an ongoing process for identifying, 
evaluating and managing the significant 
risks the Group faces. 

The Board delegates to the Executive team 
the responsibility for designing, operating 
and monitoring both the risk management 
and internal control systems, and the 
maintenance of effective internal controls 
within the Group. The Company also has a 
whistleblowing policy. 

The systems and controls in place include 
policies and procedures, which relate to 
the maintenance of records that fairly and 
accurately reflect transactions, correctly 
evidence and control the Group’s assets, 
provide reasonable assurance that 
transactions are recorded as necessary 
to enable the preparation of financial 
statements in accordance with International 
Financial Reporting Standards (“IFRS”), and 
review and reconcile reported results. 

The Group’s key internal controls are: 

•  an independent review of internal 
controls was completed in 2020;

•  a regular review of the Group’s 

insurance policies with its insurance 
broker to ensure that the policies are 
appropriate for the Group’s activities 
and exposures; 

•  a comprehensive system for 

consolidating financial results from 
Group companies and reporting these 
financial results to the Board; 

•  reviewing cash flow, annual revenue 
and capital forecasts regularly during 
the year, along with regular monitoring 
of management accounts and capital 
expenditure reported to the Board and 
comparisons with forecasts; 

•  financial controls and procedures, 

including in respect of bank payments, 
bank reconciliation’s and petty cash; 

•  monthly review of outstanding debtors; 

•  regular meetings of the Executive 

team; and 

•  an Audit Committee that approves 
audit plans and published financial 
information and reviews reports from 
the external Auditor arising from the 
audit and deals with significant control 
matters raised. 

The Board monitors the activities of the 
Group through regular Board meetings 
and it retains responsibility for approving 
any significant financial expenditure or 
commitment of resources.

Risk management is focused around 
the operational areas of the Group. The 
Group has a dedicated Regulatory Affairs 
and Quality Assurance Director who 
has extensive operational experience at 
senior management and board levels, 
and particularly strong experience 
in quality system development and 
regulatory compliance. He is responsible 
for a Regulatory team operating across 
the Group, working at identifying and 
prioritising operational risks and working 
with the operational teams to mitigate the 

identified risks. This work is supported by 
the risk assessment procedure in place 
across the Group, with the objective 
to ensure that risk assessment of the 
Group’s equipment, procedures and 
processes is approached consistently 
across the Group. 

With the assistance of the Audit 
Committee, the Board’s review process 
is principally based on reviewing regular 
reports from the Executive team to 
consider whether significant risks are 
identified, evaluated, managed and 
controlled effectively, and whether any 
significant weaknesses are promptly 
remedied. The system is designed to 
manage rather than eliminate the risk 
of failure to achieve the Company’s 
objectives, and can only provide 
reasonable and not absolute assurance 
against material misstatement or loss. 

In assessing what constitutes reasonable 
assurance, the Board considers the 
materiality of financial and non-financial 
risks and the relationship between the 
cost of, and benefit from, internal control 
systems. 

Details of the principal risks currently 
facing the Group and how they are 
mitigated are set out on pages 66 to 72. 

The Board confirms that it has, during the 
reporting period, reviewed on an ongoing 
basis the effectiveness of the Company’s 
system of internal controls including 
financial, operational and compliance 
controls and risk management systems 
and has reviewed insurance provisions. 
No significant failing or weaknesses have 
been identified.

Maintain a dynamic 
management framework 

5.  Maintain the Board 

as a well-functioning, 
balanced team led by 
the Chair 

The Chairman, James Wakefield, is 
responsible for leadership of the Board, 
ensuring its effectiveness in all aspects of 
its role. The Company is satisfied that the 
current Board is sufficiently resourced to 
discharge its governance obligations on 
behalf of all stakeholders.

To enable the Board to discharge its 
duties, all Directors receive appropriate 
and timely information. Briefing papers 
are distributed to all Directors in advance 
of Board and Committee meetings. 
All Directors have access to the advice 
and services of the Chief Financial 

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principles  

continued

Officer and the Company Secretary, 
who are responsible for ensuring that 
the Board procedures are followed, and 
that applicable rules and regulations are 
complied with. In addition, procedures are 
in place to enable the Directors to obtain 
independent professional advice in the 
furtherance of their duties, if necessary, at 
the Company’s expense. 

In between Board meetings, the Executive 
Directors maintain regular informal contact 
with the Non-Executive Directors. Whilst 
the Board retains overall responsibility 
for, and control of, the Group, day-to-
day management of the business is 
conducted by the Executive Directors, 
who meet with the senior management 
team on a weekly basis. 

Board of Directors
The composition of the Board during the 
period is summarised in the table on page 
43 of the Directors’ Report. As at the date 
of this Report, the Board comprises seven 

members, of which five are Non-Executive 
Directors, all of whom are independent, 
namely James Wakefield, Andrew Heath, 
Dr Ed Snape, Juliet Thompson and  
Jean-Pierre Crinelli.

Independence of Directors
The Directors acknowledge the 
importance of the principles of the 
QCA Code that recommend that a 
company should have at least two 
independent non-executive directors. 
The Board has, therefore, considered 
and determined that, since the date of 
their respective appointments, James 
Wakefield, Dr Andrew Heath, Dr Ed 
Snape, and Juliet Thompson were, 
and continue to be, independent of the 
Executive management and free from any 
relationship that could materially affect the 
exercise of their independent judgement.

At the time of the AIM listing, Jean-Pierre 
Crinelli’s role had just changed to that 
of a Non-Executive Director. At that 
time, the Board did not consider him 
independent as he was previously an 
Executive Director of the Company and 
one of the founders of the NOVAprep® 
business. The Board now considers 
Jean-Pierre Crinelli to be an Independent 
Non-Executive Director. It has reached 
this view following the sale of NOVAprep® 
by the Company in 2019, and because 
he has now been a Non-Executive 
Director for over five years, and has 
demonstrated his independence over 
that period through his questioning at 
Board meetings. All other Non-Executive 
Directors are considered independent 
for the purpose of the QCA Code, as 
none have beneficial or non-beneficial 
shareholdings in the Company exceeding 
3%, nor have an existing tenure of more 
than 12 years. Dr Ed Snape is a co-
owner of Nexus Medical, LLC, the general 

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50

partner of Nexus Medical Partners II, L.P., 
which has a current shareholding in the 
Company of less than 3% Accordingly, Dr 
Ed Snape is considered by the Directors 
to be independent for the purposes of the 
QCA Code.

All the Non-Executive Directors 
constructively challenge and help develop 
proposals on strategy and bring strong, 
independent judgement, knowledge and 
experience to the Board’s deliberations. 
The Non-Executive Directors are of 
sufficient experience and competence 
that their views carry significant weight in 
the Board’s decision making and when 
relevant, would record their concerns 
about the running of the Company. At 
each meeting, the Board considers 
Directors’ conflicts of interest. 

The Non-Executive Directors have regular 
opportunities to meet without Executive 
Directors being present (including time 
after Board and Committee meetings).

Time commitments
Non-Executive Directors receive a formal 
appointment letter on joining the Board, 
which identifies the terms and conditions 
of their appointment.

A potential director candidate (whether 
an executive director or non-executive 
director) is required to disclose all 
significant outside commitments prior to 
their appointment.

The Board is satisfied that both the 
Chairman and the Non-Executive 
Directors are able to devote sufficient time 
to the Company’s business.

If considered appropriate, the Board 
may authorise Executive Directors to 
take non-executive positions in other 
companies and organisations, provided 
the time commitment does not conflict 
with the Director’s duties to the Company, 
since such appointments should broaden 
their experience. The acceptance of 
appointment to such positions is subject 
to the approval of the Chairman.

Attendance at Board and 
Committee meetings
The Directors meet at least ten times per 
year for formal Board meetings to discuss 
and decide the Group’s business, financial 
performance and strategic decisions. 
In addition, and as required, the Board 
meets more frequently by conference 
call to discuss and decide on matters 
considered more urgent, such as those 
relating to acquisitive growth. 

During the reporting period, the Board 
met in person or via conference calls 16 
times.

In advance of each meeting of the 
Directors, the Board is provided with 
relevant information to ensure that it 
can properly carry out its role. For each 
meeting, the Directors generally consider 
the minutes of the previous meeting and 
any action points, recent forecast and 
operations, cash flows and progress on 
any particular projects.

The attendance of each Director at Board and Committee meetings during the period is set out in the table below. Attendance 
is expressed as the number of meetings attended/number eligible to attend. Directors’ attendance by invitation at meetings of 
Committees of which they are not a member is not reflected in the following table.

Director

James Wakefield

Graham Mullis

Anthony Dyer

Dr Andrew Heath

Dr Edwin Snape

Jean-Pierre Crinelli

Juliet Thompson

Board

16/16

16/16

16/16

16/16

16/16

16/16

16/16

Audit Committee

Nomination Committee

Remuneration Committee

–

–

–

5/5

–

5/5

5/5

2/2

–

–

2/2

–

–

2/2

–

–

–

9/9

9/9

–

9/9

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principles  

continued

6.  Ensure that, between 

them, the Directors have 
the necessary up-to-
date experience, skills 
and capabilities

The Board currently comprises two 
Executive and five Non-Executive 
Directors with an appropriate balance of 
sector, financial and public market skills 
and experience to deliver the Group’s 
strategy for the benefit of Shareholders 
over the medium to long term. The 
Board considers that the Non-Executive 
Directors bring a wide experience at 
a senior level of business operations 
and strategy and have an expanse of 
knowledge and expertise gained from 
other areas of business. 

The skills and experience of the Board 
are set out in their biographical details 
on pages 38 to 41. The experience 
and knowledge of each of the Directors 
gives them the ability to constructively 

challenge the strategy and to scrutinise 
performance. The Board also has access 
to external advisors where necessary. 
Neither the Board nor its Committees 
sought external advice on any significant 
matter during the reporting period.

New Directors are presented with 
appropriate levels of background 
information on the Company, meet the 
management, visit sites and spend time 
with the Chairman and other Directors as 
required. The induction is tailored to meet 
each new Director’s specific needs. 

Throughout their period in office, the 
Directors are continually updated on 
the Group’s business, the industry and 
competitive environment in which it 
operates, corporate social responsibility 
matters and other changes affecting the 
Group by written briefings and meetings 
with senior executives. 

Each Director takes responsibility for 
maintaining their skill set, which includes 
roles and experience with other boards 
and organisations as well as attending 
formal training and seminars. 

The Executive Directors receive regular 
and ongoing updates from their 
professional advisors covering financial, 
legal, tax and the Euronext Growth Paris 
and AIM Rules.

The Company Secretary provides 
information and advice on corporate 
governance and individual support to 
Directors on any aspect of their role, 
particularly supporting the Chairman and 
those who chair Board Committees. The 
Company Secretary is also responsible 
for ensuring that Board procedures are 
followed, that the Company complies 
with company law and with the Euronext 
Growth Paris and AIM Rules. 

The Company is a strong supporter of 
diversity in the boardroom and, during the 
reporting period, the Board comprised 
one female and six male Directors. The 
Company remains of the opinion that 
appointments to the Board should be 
made relative to a number of different 
criteria including diversity of gender, 
background and personal attributes, 
alongside the appropriate skill set, 
experience and expertise.

7.  Evaluate Board 
performance 
based on clear and 
relevant objectives, 
seeking continuous 
improvement

Board evaluation
The Board is mindful that it needs to 
continually monitor and identify ways in 
which it might improve its performance 
and recognises that Board evaluation 
is a useful tool for enhancing a Board’s 
effectiveness. As a matter of course, 
alongside the annual evaluation, the 
Chairman routinely assesses the 
performance of the Board and its 
members and discusses any issues, 
problems or shortcomings with the 
relevant Director(s). Likewise, the Senior 
Independent Director reviews the 
performance of the Chairman.

It is not an AIM requirement for 
an external Board appraisal to be 
undertaken; however, in view of the 
significant growth experienced by the 
Company during 2020 and its growth 
plans for the future, the Board intends 
to appoint an external third party to 
undertake an independent review of the 
Board and its operations. The report will 
seek input from all Board members both 
in the form of a questionnaire and one-to-
one interviews covering:

•  the themes from the questionnaire;

•  the assessment of the Director’s 
individual performance; and

•  feedback on Board colleague’s 

individual performance.

In addition, the independent review will 
have access to certain historic non-
confidential/price sensitive Board packs 
and other information.

Final feedback will be in the form of a 
full report for internal use. It is intended 
that this includes an Executive summary 
and key findings, together with a 

detailed analysis of the responses to the 
questionnaire and anonymised comments 
made in response to the questionnaire 
and during the interviews. The report 
will also include recommendations for 
consideration together with benchmarking 
against best practice.

The aim of the review is to ensure that 
the Board contains the necessary skills to 
enable it to be satisfied that:

•  the Board continues to meet its 

regulatory requirements and ensures 
that appropriate processes are in place 
for setting the strategic direction of the 
Group; 

•  each Committee continues to be 

effective and that all members were 
considered to have made valuable 
contributions, and individual Directors 
continue to perform effectively; and

•  feedback will be provided through 
the Chairman to individual Board 
members.

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principles  

continued

8.  Promote a corporate 
culture that is based 
on ethical values and 
behaviours 

The Company recognises the importance 
of investing in its employees to provide 
foundations and leadership to drive 
performance further regardless of age, 
race, religion, gender or sexual orientation 
or disability. Our core Company values 
are the building blocks for developing our 
dynamic and challenging culture within 
the Group.

These values represent our philosophy 
which through our people and 
organisation will help the business deliver 
our Company goals. The values represent 
how each of us can contribute to the 
success of the Company both now and in 
the future as an individual and also as part 
of the wider team.

•  To treat each other with trust, dignity 

and respect.

•  Enabling, empowering and energising 

others to make things happen.

•  Work as a team with colleagues and 

across functions.

•  Innovation, inspiration and motivation, 

creating an open culture where people 
are valued for their contribution.

•  Novacyt endeavours to deliver the best 
quality service to all of our internal and 
external customers.

The Group recognises the importance of 
investing in its employees and, as such, 
the Group provides opportunities for 
training and personal development and 
encourages the involvement of employees 
in the planning and direction of their 
work. These values are applied regardless 
of age, race, religion, gender, sexual 
orientation or disability.

The Group believes that it has robust 
policies and procedures for combating 
bribery and corruption. A copy of the 
Group’s Anti-Corruption and Bribery 
Policy can be found on the Group’s 
website www.novacyt.com. 

The Group recognises that commercial 
success depends on the full commitment 
of all its employees and commits to 
respecting their human rights, to provide 
them with favourable working conditions 
that are free from unnecessary risk and 
to maintain fair and competitive terms 
and conditions of service at all times. 
The performance and reward system 
endorses the desired ethical behaviours 
across all levels of the Group.

9.  Maintain governance 

structures and 
processes that are fit for 
purpose and support 
good decision making 
by the Board 

The Chairman, James Wakefield, is 
responsible for leading the Board, 
facilitating the effective contribution 
of all members and ensuring that it 
operates effectively in the interests of 
the Shareholders. Graham Mullis, the 

Chief Executive Officer, is responsible 
for the leadership of the business and 
implementation of the strategy. By 
dividing responsibilities in this way, no 
one individual has unfettered powers of 
decision making.

The Board reserves for itself a range of 
key decisions to ensure that it retains 
proper direction and control of the Group, 
and a formal schedule of matters reserved 
for decision by the Board has been 
adopted by the Board since admission 
to AIM; a copy of which can be found at 
www.novacyt.com. Such matters include 
business strategy and management, 
financial reporting (including the approval 
of the annual budget), Group policies, 

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principles  

continued

corporate governance matters, major 
capital expenditure projects, material 
acquisitions and divestments and the 
establishment and monitoring of internal 
controls. This schedule may be updated 
by the Board and approved by the Board 
only. The day-to-day management of 
the business has been delegated to the 
Chief Executive Officer and the wider 
Executive team.

The appropriateness of the Board’s 
composition and corporate governance 
structures are reviewed through the 
ongoing Board evaluation process and on 
an ad hoc basis by the Chairman together 
with the other Directors, and these 
will evolve in parallel with the Group’s 
objectives, strategy and business model 
as the Group develops.

Board Committees
The Board has established an Audit 
Committee, a Remuneration Committee 
and a Nomination Committee; the terms 
of these Committees reflect market 
practice on AIM. These Committees 
of the Board have formally delegated 
responsibilities.

Copies of each Committee’s terms of 
reference are available on the Company’s 
website at www.novacyt.com. 

Audit Committee
The Audit Committee is chaired by Juliet 
Thompson, and has primary responsibility 
for monitoring the quality of internal 
controls, ensuring that the financial 
performance of the Group is properly 
measured and reported on, and for 
reviewing reports from the Group’s auditor 
relating to the Group’s accounting and 
internal controls, in all cases having due 
regard to the interests of Shareholders. 
The Audit Committee meets at least twice 
a year. Dr Andrew Heath and Jean-Pierre 
Crinelli are the other members of the Audit 
Committee. 

A report on the duties of the Audit 
Committee and how it discharges its 
responsibilities is provided on pages  
62 to 65.

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Remuneration Committee
The Remuneration Committee is chaired 
by Dr Andrew Heath, and reviews the 
performance of the Executive Directors, 
and determines their terms and conditions 
of service, including their remuneration 
and the grant of options, having due 
regard to the interests of Shareholders. 
The Remuneration Committee meets at 
least twice a year. Dr Ed Snape and Juliet 
Thompson are the other members of the 
Remuneration Committee. 

The Directors’ Remuneration Report and 
details of the activities and responsibilities 
of the Remuneration Committee are set 
out on pages 58 to 61. 

Nomination Committee
The Nomination Committee is chaired 
by James Wakefield, and identifies and 
nominates, for the approval of the Board, 
candidates to fill Board vacancies as 
and when they arise. The Nomination 
Committee meets at least once a year. 
Dr Andrew Heath and Juliet Thompson 
are the other members of the Nomination 
Committee. 

Details of the activities and responsibilities 
of the Nomination Committee are set out 
on page 57. 

Build trust

10.  Communicate how the 
Company is governed 
and is performing

As explained earlier in this Corporate 
Governance Statement, the Board has 
established a Nomination Committee, an 
Audit Committee and a Remuneration 
Committee. The work of each of the 
Board Committees undertaken during the 
year ended 31 December 2020 is detailed 
on pages 57 to 65. 

The Board places its responsibility to the 
Company’s Shareholders and setting the 

Nomination  
Committee Report

The Company 
established 
a Nomination 
Committee during 
2017 prior to its 
admission onto the 
AIM market

James Wakefield acts as Chairman of 
the Nomination Committee and its other 
members are Juliet Thompson and 
Dr Andrew Heath. All members of the 
Nomination Committee are considered 
independent.

The Nomination Committee is responsible 
for identifying and nominating for the 
approval of the Board candidates to fill 
Board vacancies as and when they arise, 
and to ensure that the Board consists 
of members with the range of skills and 

qualities needed to meet its principal 
responsibilities in a way that promotes the 
protection of the interests of stakeholders 
and compliance with the requirements of 
the AIM Rules.

The Nomination Committee will meet at 
least once a year and at such other times 
as the Chairman or any other member of 
the Nomination Committee requires.

Group’s strategy for achieving long-term 
success as a high priority. The Group’s 
website is regularly updated with all press 
releases, AGM and EGM results and 
investor presentations.

The results of the votes received in 
relation to the 2020 AGM and EGM are 
available on the Company’s website. 
All resolutions were passed at the 2020 
General Assembly and no resolution had 
a significant proportion (>20%) of votes 
cast against them at that meeting. 

The Board maintains a healthy dialogue 
with all of its stakeholders. Throughout 
the course of the year, the Board 
communicates with Shareholders directly 
on any views, concerns and expectations 
they may wish to express. 

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Remuneration Report

Remuneration  
Committee

As Chairman of the Remuneration 
Committee, I am pleased to present our 
Directors’ Remuneration Report for the 
year ended 31 December 2020.

This report does not constitute a 
Directors’ remuneration report in 
accordance with the Companies Act 
2006. As a Company whose shares are 
admitted to trading on AIM, the Company 
is not required by the Companies 
Act to prepare such a report. We do, 
however, have regard to the principles 
of the QCA Code, which we consider 
to be appropriate for an AIM company 
of our size. The report provides a 
general statement of policy on Directors’ 
remuneration as it is currently applied, 

and details the remuneration for all 
Directors during the year. It also provides 
a summary of the Novacyt LTIP, which 
was established during 2017 and vested 
in 2020.

Dr Andrew Heath
Chairman of the Remuneration Committee

Dr Andrew Heath
Chairman of the Remuneration 
Committee

Key responsibilities
The Remuneration Committee determines 
performance-related targets for the 
members of the Executive team, 
reviews their performance and makes 
recommendations to the Board on 
matters relating to their remuneration and 
terms of employment.

The Remuneration Committee also 
makes recommendations to the Board 
on proposals relating to all long-term 
incentive scheme structures and any 
future option schemes, and the granting 
of any share options under such 
schemes. The remuneration and terms 
and conditions of appointment of the 
Non-Executive Directors are set by the 
Board.

Composition and 
meetings
The Remuneration Committee comprises 
at least two members, and all members 
are Non-Executive Directors considered 
independent. Dr Andrew Heath acts 
as Chairman of the Remuneration 
Committee, and Dr Edwin Snape and 
Juliet Thompson are the other members.

Only members of the Remuneration 
Committee have the right to attend 
meetings, but other Directors and external 
advisors may be invited to attend all 
or part of any meeting as and when 
appropriate. No Director may be involved 
in discussions relating to their own 
remuneration.

The Remuneration Committee meets 
as appropriate but not less than twice a 
year. During the period, the Remuneration 
Committee met nine times. Details of 
meeting attendance are shown in the 
table in the Corporate Governance 
Statement on page 51.

1.  Executive team salaries and short-term 
bonuses were reviewed and agreed.

Policy on Executive 
remuneration
The Remuneration Committee is 
responsible for determining and agreeing 
with the Board the framework or broad 
policy for the remuneration of the 
Executive team. In determining such 
policy, the Remuneration Committee 
takes into account all factors that it deems 
necessary including the relevant legal and 
regulatory requirements and corporate 
governance guidelines. The Remuneration 
Committee also takes into account 
emerging best practice and guidance 
from major institutional Shareholders. The 
objective of the Company’s remuneration 
policy is to attract, retain and motivate 
individuals of the quality required to 
run the Company successfully without 
paying more than is necessary, having 
regard to views of shareholders and other 
stakeholders.

The Remuneration Committee recognises 
that the remuneration policy should 
have regard to the risk appetite of 
the Company and alignment to the 
Company’s long-term strategic goals, with 
a significant proportion of remuneration 
being structured to link rewards to 
corporate and individual performance, 
designed to promote the long-term 
success of the Company.

The Remuneration Committee, when 
setting the remuneration policy for 
Executive Directors, also has regard to the 
pay and employment conditions across 
the Group, particularly when conducting 
salary reviews.

The main elements of the remuneration 
packages of the Executive Directors are 
as follows.

Basic annual salary  
and pension
Basic salary is reviewed annually by 
the Remuneration Committee, usually 
in February, and takes into account a 
number of factors, including the current 
position and progress of the Group, 
individual contribution and market salaries 
for comparable organisations.

The Company makes contributions 
into the private pension schemes of the 
Executive Directors.

Discretionary bonus
At the discretion of the Remuneration 
Committee, taking into account 
performance against certain financial and 
individual targets, an Executive Director 
may be entitled to an annual discretionary 
cash bonus on such terms and subject 
to such conditions as may be decided 
from time to time by the Remuneration 
Committee. 

The Novacyt LTIP 2017 to 2020
The Board of Novacyt established and 
adopted an LTIP scheme on 17 October 
2017 as an alternative to more standard 
long-term incentive plans. Due to 
the complexities of being a French 
incorporated company with a UK-based 
management, it proved difficult at the 
time of admission to establish a standard 
equity-based long-term incentive plan.

Executive Directors and certain senior 
employees of the Group were eligible to 
participate in the Novacyt LTIP.

The Novacyt LTIP was designed to give 
participants the right to receive a cash 
amount that was calculated based on the 
growth in value of a specified number of 
ordinary shares over a specified period of 
time. The Novacyt LTIP therefore allowed 
the Company to grant to qualifying 
employees a phantom award over a 
defined number of notional ordinary 
shares (a ‘‘Phantom Award’’).

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Committee  

continued

These Phantom Awards were subject 
to performance or other conditions so 
that the Phantom Awards would not vest 
unless any such condition(s) had been 
satisfied or waived. Any performance 
conditions were objective and determined 
by the Board before Phantom Awards 
were granted.

The Phantom Awards vested on the third 
anniversary of the date of grant, that being 
1 November 2020, upon performance 
condition(s) applying to the Phantom 
Award being met. On the Vesting Date, 
the amount of the award was calculated 
with the final amount being equal to the 
difference between the closing price of 
an ordinary share on the Vesting Date 
and the closing price of an ordinary share 
on the date of grant, multiplied by the 
number of notional ordinary shares over 
which the Phantom Award had vested.

Performance during the term resulted in 
full vesting of the LTIP awards granted 
in November 2017. The Remuneration 
Committee believes this vesting outcome 
is reflective of the strong performance of 
the Company. However, both Graham 
Mullis and Anthony Dyer took a voluntary 
23% and 18% respectively decrease in 
their award. The voluntary decrease was 
agreed by management with the Board 
and some of this reduction is being used 
to support the Company’s charitable 
donation programme for 2021, which is 
described on page 35. The exact sums 
paid are reflected in the remuneration 
table on page 60.

Payment of the calculated amount will be 
made in three tranches on the third, fourth 
and fifth anniversary of the date of grant 
(each, a ‘‘Payment Date’’) and satisfied  
in cash.

Payment of any tranche of the award will, 
in each case, be subject to the Company’s 
ability to make the payment and the 
employee’s continued employment on the 
relevant Payment Date.

Benefits in kind
Executive Directors are entitled to benefits 
in kind commensurate with their position, 
including company car allowance, private 
medical and death in service insurance.

Directors’ remuneration
The remuneration of the Directors who served on the Company’s Board during the year to 31 December 2020 was as follows:

Year ended 31 December 2020

Year ended 31 December 2019

Basic 
salary and 
fees

Bonus

Pension

LTIP

Total

Basic 
salary and 
fees

Bonus

Pension

Total

Executive Directors

Graham Mullis

Anthony Dyer

Non-Executive Directors

Jean-Pierre Crinelli*

James Wakefield

Andrew Heath

Juliet Thompson

Edwin Snape**

322,263

264,341

20,327 8,204,196*** 8,811,127  265,188

45,000

17,369 327,557

175,868

65,922

8,873 2,905,650***  3,156,313 168,300

15,000

8,690 191,990

35,767

90,000

43,875

43,875

28,053

–

–

–

–

–

–

–

–

–

–

–

–

–

–

–

35,767

26,300

90,000

55,000

43,875

40,000

43,875

40,000

28,053

23,492

–

–

–

–

–

–

–

–

–

–

26,300

55,000

40,000

40,000

23,492

 Salaries paid in Euros and disclosed in GBP, translated at the average exchange rate of 1.125107 in 2020 (2019: 1.140645).  

* 
**   Salary paid in USD and disclosed in GBP, translated at the average exchange rate of 1.28360 in 2020 (2019: 1.276989). 
*** 1/3 received in 2020, the following two payments are deferred with payments in 2021 and 2022.  

Directors’ shareholdings and share interests 
The interests of the Directors who served during the year in the share capital of the Company as of 31 December 2020, 31 December 
2019 and the date of this report were as follows:

Graham Mullis and family

Anthony Dyer

James Wakefield

Dr Andrew Heath and family

Dr Edwin Snape

Jean-Pierre Crinelli

Juliet Thompson

As at the date of report

31 December 2020

31 December 2019

122,506

122,506 

16,839

36,839

20,000

17,919

30,773

–

16,839

36,839

20,000

17,919

30,773

–

52,138

16,839

16,839

16,839

16,839

15,333

–

All interests are beneficially held. There is no requirement for Directors to hold shares in the Company. 

Directors’ share interests awarded from the Phantom LTIP plan 2017 to 2020
Details of the number of notional shares under Phantom Awards granted under the Novacyt LTIP to Directors who served during the 
year are set out in the table below:

Director

Graham Mullis

Anthony Dyer

Granted during 
2017

Satisfied during 
the period

Lapsed during the 
period

1,129,930

1,129,930

376,643

376,643

–

–

These Phantom Awards vested at the closing price on the Vesting Date, having met the performance condition that the closing price 
of a Share, averaged over 30 consecutive dealing days prior to the Vesting Date, exceeded €0.66 per share, being the Placing Price 
upon admission to AIM

Conclusion
This report is intended to explain clearly the remuneration approach adopted by the Company and to enable Shareholders to 
appreciate how it underpins the Group’s business growth and strategic objectives. The Board considers that the current remuneration 
policy is fair and is fully aligned with the interests of Shareholders.

Dr Andrew Heath
Chairman of the Remuneration Committee 

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Report

Juliet Thompson
Chair of the Audit Committee

The Audit Committee comprises at 
least two members, with at least one 
Non-Executive Director considered 
independent, including the Chairman. 

In addition, the Chief Financial Officer and 
other members of the Executive team 
may be invited to attend as required.

Independent Non-Executive Director, 
Juliet Thompson, being a chartered 
accountant, acts as Chair of the Audit 
Committee, and its other members are 
Jean-Pierre Crinelli and Dr Andrew Heath.

Summary of the role of 
the Audit Committee
The Audit Committee’s primary 
responsibility is to monitor the quality 
of internal controls and ensure that the 
financial performance of the Group is 
properly measured and reported on.

It receives and reviews reports from the 
Executive team and external Auditors 
relating to the interim and annual 
accounts and the accounting and internal 
control systems in use throughout the 
Group.

The Audit Committee meets as 
appropriate, but not less than twice a 
year, and minutes are recorded for each 
meeting by the Chief Financial Officer. 
The Audit Committee is able to call for 
information from the Executive team and 
has unrestricted access to the Company’s 
external Auditors.

The Audit Committee operates within 
specific terms of reference that include:

•  Reviewing management procedures 
to monitor the effectiveness of the 
accounting systems, accounting 
policies and internal controls;

•  Conducting a regular and ongoing 

process of risk assessment;

•  Reviewing the scope and planning of 

the external audit;

•  Reviewing the findings of the external 
Auditor and management’s response;

•  Reviewing the annual financial 

statements before their submission to 
the Board for approval;

•  Making recommendations to the Board 

concerning the appointment and 
remuneration of the external Auditor;

•  Reviewing any profit forecasts or 

working capital statements published 
in any bid document or listing 
particulars as investigated and verified 
by the Company’s auditor and/or 
reporting accountant;

•  Reviewing from time to time the cost 
effectiveness of the audit including 
a review of the performance of the 
external Auditor;

•  Monitoring the fees paid to the external 
Auditor and where the external Auditor 
supplies a substantial volume of non- 
audit services to the Company, to keep 
the nature and extent of such services 
under review, in order to achieve a 
balance between objectivity and value 
for money; and 

•  Having the right to obtain outside legal 
help and any professional advice, at 
the Company’s expense, which might 
be necessary for the fulfilment of its 
duties.

The Audit Committee is responsible 
for ensuring the ‘right tone at the top’ 
and that the ethical and compliance 
commitments of the Executive team 
and other employees are understood 
throughout the Group.

External Auditors
The Audit Committee is responsible for 
making recommendations to the Board 
on the appointment, reappointment 
and removal of the external Auditor and 
assesses annually the qualifications, 
expertise, resources, remuneration and 
independence of the external Auditor. The 
Audit Committee receives reports on the 
external audit firm’s own internal quality 
control procedures and confirmation of 
the Auditor’s independence. The Audit 
Committee ensures that appropriate plans 
are in place for the external Auditor each 
annual cycle.

The Group’s external Auditor is Deloitte 
LLP. Under French law, the mandatory 
term for auditors is six years. Deloitte 
LLP was reappointed as external Auditor 
during the AGM held in 2018 and has 
now been the Auditor for nine years at the 
end of the audit of the annual accounts 
for the year ended 31 December 2020.

The Audit Committee annually reviews 
the effectiveness of the external Auditor. 
This process involves overseeing the 

relationship with the Group’s external 
Auditor, including reporting to the Board 
each year whether it considers the audit 
contract should be put out to tender, 
adhering to any legal requirements for 
tendering or rotation of the audit services 
contract as appropriate, reviewing 
and monitoring the external Auditor’s 
objectivity and independence, agreeing 
the scope of their work and fees paid 
to them for audit, and assessing the 
effectiveness of the audit process. The 
external Auditor presents to the Audit 
Committee the output of its detailed 
year-end work and the Audit Committee 
challenges significant judgements 
(if any). In making its assessment of 
external Auditor effectiveness, the Audit 
Committee reviews the audit engagement 
letters before signature, reviews the 
external Auditor’s summary of Company 
issues, and conducts an overall review 
of the effectiveness of the external audit 
process and the external Auditor. The 
Audit Committee reports its findings to 
the Board.

The Audit Committee and the Board have 
been satisfied with the performance of the 
external Auditor during the year and with 
the policies and procedures they have 
in place to maintain their objectivity and 
independence.

The Audit Committee also approves in 
advance any non-audit services to be 
performed by the Auditor such as tax 
compliance and advisory work, audit-
related assurance services (e.g. reviews 
of internal controls and reviewing the 
Group’s interim financial statements).

Any non-audit services that are to 
be provided by the external Auditor 
are reviewed in order to safeguard 
Auditor objectivity and independence.  
Accordingly, the Board can confirm 
that, during the reporting period, there 
have been no non-audit services that 
are considered to have impaired the 
objectivity and independence of the 
external Auditor. A full breakdown of 
payments made to the external Auditor 
during the financial year is disclosed 
within note 47 to the financial statements.

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Report  

continued

Work undertaken by  
the Audit Committee 
during the period
The Audit Committee met five times 
during the period. Details of meeting 
attendance are shown in the Corporate 
Governance Statement on page 51.

•  Review of the Company’s interim report 

for the six months ended 30 June 
2020;

•  Approval of the audit fees for the 

financial year ended 31 December 
2020;

•  Approval of non-audit work to be 

carried out by the Auditor;

Deloitte LLP, as the Auditor, was also 
present at one of the meetings.

•  Consideration of the independence 

and objectivity of the external Auditor;

The key matters considered by the Audit 
Committee whilst discharging its duties 
and responsibilities are set out below:

•  Review of the internal controls and 
risk management systems within 
the Group;

•  Review of the Annual Report and 

Accounts for year ended 31 December 
2019;

•  Consideration and approval of the 

unaudited interim financial statements 
for the period ended 30 June 2020;

•  Review of the financial integrity of the 
Group’s financial statements including 
relevant corporate governance 
statements;

•  Consideration of the requirement for 
the Group to have an internal audit 
function;

•  Review of the effectiveness of 

the external Auditor, as more fully 
described above;

•  Discussions with the Auditor on the 

audit approach and strategy, the audit 
process, significant audit risks and 
key issues of focus for the annual 
audit; and

•  Review and approval of the continuing 
appointment of Deloitte LLP as the 
Group’s Auditor.

The ultimate responsibility for reviewing 
and approving the financial statements 
in the interim and annual reports remains 
with the Board.

The Audit Committee, in conjunction 
with the Auditor, has considered there 
are no significant issues relating to the 
preparation of the financial statements 
contained in this Annual Report.

Risk management and 
internal control
The Board has overall responsibility for 
the Group’s system of internal control and 
for reviewing the effectiveness of internal 
control to safeguard Shareholders’ 
investment and the Group’s assets. There 
is an ongoing process for identifying, 
evaluating and managing the significant 
risks the Group faces. The Board regularly 
reviews the process, which has been in 
place throughout the period and up to 
the date of approval of the Annual Report 
and Accounts.

The Board’s internal control and risk 
management review process (conducted 
with the assistance of the Audit 
Committee), is outlined on pages 62 to 65.

Internal audit
The Board has reviewed the need 
for a separate internal audit function 
and concluded that such a function 
is not currently appropriate for a size 

of company such as the Group, and 
because the internal audit principles 
already fall under the remit of the 
Audit Committee.

Going concern
The Directors have, at the time of 
approving the financial statements, a 
reasonable expectation that the Group 
has adequate resources to continue in 
operational existence for the foreseeable 
future. Thus, they adopt the going 
concern basis of accounting in  
preparing the financial statements.

The going concern model covers the 
period up to and including June 2022. 
In making this assessment, the Directors 
have considered the following elements:

•  The working capital requirements of 

the business;

•  A positive cash balance at 31 

December 2020 of £91,765,000;

•  Payment of the second tranche of the 

Long-Term Incentive Plan (“LTIP”) that 
commenced in November 2017;

•  Payment of the first earn-out milestone 

related to the IT-IS International 
acquisition; and

•  Management’s confidence in settling 

the outstanding commercial dispute as 
per note 50 in the Group accounts.

In the event the current dispute is fully 
settled in favour of the counterparty, 
the forecast prepared by the Group 
shows that it is able to cover its cash 
needs during the financial year 2021 
and until June 2022 without the raising 
of any banking or other financing facility.
Approved by on behalf of the Board.

Juliet Thompson
Chair of the Audit Committee 

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Risk Management

The Group’s risk management strategy is a key responsibility of 
the Board of Directors. The Board ensures that all major risks are 
understood and appropriately managed in light of the Group’s 
strategy and objectives, and is satisfied that the Group’s risk 
management and internal control systems are adequate.

The Group’s risk management framework supports the risk assessment procedure across the Group, with the objective of ensuring 
that the assessment of the strategic, operational, financial and external risks of the Group is approached consistently Group-wide.

At this stage of the Company’s development, the Board does not consider it to be appropriate to establish an internal audit function, 
but this will be kept under review.

The principal risks faced by the Group are set out below.

The pace of 
development in the 
healthcare industry

The Group operates within the biotechnology sector, a complex area of the healthcare 
industry. Rapid scientific and technological change within the biotechnology sector 
could lead to other market participants creating approaches, products and services 
equivalent or superior to the diagnostic testing products and services offered by 
the Group, which could adversely affect the Group’s performance and success. If 
the Group is unable to keep pace with these changes in the biotechnology sector 
and in the wider healthcare industry, the demand for its technological platforms and 
associated products and services could fall.

Competitive pressures

Companies operating within the biotechnology sector are subject to competitive forces 
that may result in price discounting and product obsolescence.

Better resourced competitors may be able to devote more time and capital towards 
the R&D process, which, in turn, could lead to scientific and/or technological 
breakthroughs that may materially alter the outlook or focus for markets in which the 
Group operates.

In addition, a certain number of the Group’s competitors may have significantly greater 
financial and human resource capacity and, as such, better manufacturing capability 
or sales and marketing expertise. Competitors could also resort to price discounting 
or other sales and marketing strategies. Equally, new companies with alternative 
technologies and products may also emerge.

The Group is largely based in the UK, and its products are distributed to and sold 
across multiple jurisdictions. In each of these jurisdictions, there may be a number 
of associated risks in respect of which the Group will have no, or limited, control. 
These may include: contract renegotiation, contract cancellation, economic, social or 
political instability or change, hyperinflation, currency non-convertibility or instability, 
and changes of laws affecting foreign ownership, taxation, working conditions, rates of 
exchange, exchange control and licensing.

Geographic markets

Product development

Additional products and services developed through the element of the Group’s 
strategy focused on R&D transformation will be required to drive the Group’s growth, 
such as Primerdesign’s focus on transferring assays from RUO to clinical CE-IVD 
products. The development of such additional diagnostic testing products and services 
may take longer than expected or not be successful at all, which may adversely 
impact the Group’s ability to generate revenues and achieve sustainable profitability. 
In addition, the value of additional diagnostics tests and products may not prove as 
robust as currently envisaged by the Group. Any delays or unbudgeted expenditures 
incurred by the Group could postpone or halt the commercialisation of a particular 
diagnostics tests and products.

Product liability claims

The Group faces an inherent risk of product liability and associated adverse publicity as 
a result of the sales of its products.

Criminal or civil proceedings might be filed against the Group by patients, the 
regulatory authorities, pharmaceutical companies and any other third party using or 
marketing its products. Any such product liability claims may include allegations of 
defects in manufacturing, defects in design, negligence, strict liability, a breach of 
warranties and a failure to warn of dangers inherent in the product.

If the Group cannot successfully defend itself against product liability claims, it may 
incur substantial liabilities or be required to limit commercialisation of its products, if 
approved. Even successful defence could require significant financial and management 
resources.

Although the Group maintains a level of insurance that is customary for its industry 
to cover its current business, any claim that may be brought against the Group could 
result in a court judgement or settlement in an amount that is not covered, in whole or 
in part, by its insurance or that is in excess of the limits of its insurance coverage.

Its insurance policies also have various exclusions and the Group may be subject to a 
product liability claim for which the Group has no coverage.

Due to the specific and innovative nature of some of the Group’s products, there 
may only be a single supplier of goods or services to the Group in respect of those 
products or services, which may or may not be pursuant to the terms of exclusive 
supplier agreements. The Group’s purchases may be delayed if that single supplier, in 
respect of any one product or service, has its own manufacturing difficulties or is not 
able to meet the purchase requirements of the Group within a reasonable timeframe. 
Further, any exclusive supplier arrangements may be terminated by either the supplier 
or the Company on notice. In the event of serious delays or non-performance by 
such suppliers, or upon such arrangements being terminated, the Group’s own 
stock levels could diminish or be exhausted. The Group may consider expanding its 
current supplier base to reduce the reliance on certain suppliers. However, there is 
no guarantee that they will be successful in doing so in a manner that complies with 
regulatory requirements.

The Group uses third-party distributors in a number of its business areas. Although 
the Group enters into agreements with such distributors, it cannot ultimately control 
their actions and they may underperform or not act in the best interests of the Group. 
Furthermore, the distribution agreements may be terminated by the distributors or the 
Group. If so, and if appropriate from the Group’s strategy at that time, the Group may 
seek to find a replacement distributor but there can be no guarantee that they will be 
successful in doing so.

Reliance on sole 
suppliers

Reliance on third- 
party distributors

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Risk Management 

continued

Acquisition strategy

A core part of the Group’s strategy is to undertake acquisitions that are strategically 
complementary to its existing businesses. The success of such a strategy will depend 
on the Group’s ability to identify potential targets, complete the acquisition of such 
targets on favourable terms, including securing appropriate financing, and to generate 
value from the acquired targets. This strategy may not be successful under all or any 
market conditions. The Group may not be able to acquire targets on attractive terms or 
to generate resulting returns for Shareholders and prospective investors.

Litigation and arbitration From time to time, the Group may be subject to litigation arising from its operations, 

distribution and sales. Damages claimed, awarded, settled or paid under any litigation 
or arbitration may be material or may be indeterminate, and the outcome of such 
litigation or arbitration may have a material adverse effect on the Group’s business, 
financial condition, capital resources, results and or future operations. Please refer to 
Note 50 of the accounts regarding the ongoing DHSC dispute.

Key personnel

Tenders

Regulatory environment

The Group depends on the services of its key personnel, which includes a number of 
individuals some of whom are currently on a short notice period of three months or 
less. The Group’s ability to manage its R&D and product development activities, wider 
operations and financing will depend in large part on the efforts of its key personnel. 
The loss of services of key personnel, the inability to attract, retain and integrate 
suitably qualified personnel or delays in hiring required personnel, could delay the 
achievement of the Group’s objectives and strategy.

A proportion of the Group’s revenues stem from tenders awarded to the Group and it 
is not possible to control and/or predict the outcomes of these tender processes. The 
success of such tender awards is based upon the ability of the organisation or country 
to finance tenders, and then it is based upon the historical performance, price and 
quality of the competitors who have been invited to participate in the tender process. 
The Group may not be successful in future tender processes.

The failure to gain new business through the award of tender contracts may have a 
material adverse effect on the Group’s business, financial condition, capital resources, 
results and/or future operations.

The Group’s products are subject to various laws, regulations and standards in each 
of the jurisdictions in which products are manufactured and distributed. These laws, 
regulations and standards may change and, if the Group fails to meet those regulatory 
or other requirements, it could face delays or prohibitions on the operation of its 
business.

The Group’s ability to conduct business is predicated on being in compliance with 
all licence requirements as specified by each relevant jurisdiction. The Group may 
not continue to hold all of the necessary consents, approvals and licences required 
to conduct its business, and where new permissions are required, these may be 
delayed or not forthcoming. If any new approvals or licences are required in order for 
the Group to carry on its business, the Group could face delays or prohibitions on 
the development, manufacture, sale or distribution of its products, which may have a 
material adverse effect on the Group’s business, financial condition, capital resources, 
results and/or future operations.

New IVDR regulations

Employment laws

European General Data 
Protection Regulation

Information technology

The entire IVD industry within the EU is currently undergoing a significant regulatory 
transition from the existing In Vitro Diagnostic Directive (“IVDD”) (98/79/EC) to a new 
In Vitro Diagnostic Regulation (“IVDR”) (2017/746). There are a limited number of 
notified bodies available to IVDD manufacturers, which reflects a risk that the industry 
may not be ready when the new IVDR regulations to come into force. The cumulative 
effect of the introduction of the new regulation will be a significantly increased 
burden on the resources of IVD manufacturers to maintain regulatory compliance, 
and this could result in older products being deleted due to cost of compliance or 
the up-classification of products and the increased scrutiny by notified bodies. The 
IVDR will apply to any products sold in Europe even though the UK has left the EU. 
The UK, in turn, is applying its own regulatory regime to IVDDs, which will involve 
applying a UK certification mark for any products sold in the UK and this increases the 
regulatory burden.

The Group is also subject to various UK, French and EU regulations governing the 
Group’s relationship with employees, including such matters as the treatment of part-
time or agency workers, employers’ National Insurance contributions (or equivalent in 
France), overtime and other working conditions. A failure to comply with one or more 
regulations could result in the imposition of sanctions, including the closing of facilities 
for an indeterminate period of time or third-party litigation.

The Group is committed to ensuring compliance with European General Data 
Protection Regulation (“GDPR”). We have undertaken significant efforts to implement 
the requirements of the GDPR and ensure alignment throughout the business. Privacy 
matters, especially those relating to GDPR compliance, have Board and senior 
executive level attention, and relevant department stakeholders have undertaken 
training to ensure they drive a culture of compliance in their own teams and 
departments.

We are pleased with our efforts so far. Compliance with GDPR is, and will remain, an 
ongoing task for the Group, as it does for any company operating in this regulatory 
environment. GDPR will be tested and interpreted as time goes on and we are 
monitoring those developments to make sure we continue to improve our processes 
and remain compliant.

The Group is heavily reliant upon its information technology systems to enable it 
to manage a growing business and to service its customers online. Information 
systems are used across all aspects of the Group’s business, including R&D, product 
development, sales, production, stock control, distribution, and accounting and 
finance. The Group’s business would be adversely affected by a material or sustained 
breakdown in its key computer and communication systems.

In addition, the Group may face online security breaches, including hacking and 
vandalism. The Group cannot guarantee absolute protection against unauthorised 
attempts to access its information technology and communication systems, including 
malicious third-party applications that may interfere with or exploit security flaws in its 
products and services.

68
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Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNovacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationPrincipal Risks and  
Risk Management 

continued

Brexit 

Protection of intellectual 
property rights

On 23 June 2016, the UK held a referendum on the UK’s continuing membership 
of the EU, the outcome of which was a decision for the UK to leave the EU (Brexit). 
Following Royal Assent of the European Union (Withdrawal Agreement) Act on 23 
January 2020 and ratification of the Withdrawal Agreement by the European Parliament 
on 24 January 2020, the UK left the EU on 31 January 2020 and became a third 
country with a transition period running to 31 December 2020. 

As the IVDD regulations apply to all products placed on the market, we still need to 
comply with IVDD and IVDR but as we are now considered a non-EU manufacturer, we 
have to appoint a European Authorised Representative based in the EU, make labelling 
changes and register our products with an EU Competent authority. This adds cost 
and complexity to selling in Europe. In addition, the UK Government has decided not 
to recognise CE marking after 2023 and will require IVDDs placed on the UK market 
to undergo a regulatory process that duplicates the CE marking process, with a 
separate registration in the UK and the application of a UKCA mark adding further cost 
and complexity.

The Group’s ability to compete depends, in part, upon the successful protection of its 
intellectual property, in particular its patents, trademarks, know-how and trade secrets. 
The Group seeks to protect its intellectual property through the filing of worldwide 
patent and trademark applications, as well as robust confidentiality obligations on its 
employees (and any contractors).

Despite these precautions that may be taken by the Group to protect its intellectual 
technology and products, unauthorised third parties may attempt to copy, or obtain 
and use, its technology and products.

A third party may infringe upon the Group’s intellectual property, release information 
considered confidential about the Group’s intellectual property and/or claim technology 
that is registered to the Group. In addition, the Group may fail to discover infringement 
of its intellectual property, and/or any steps taken or that will be taken by it may not 
be sufficient to protect its intellectual property rights or prevent others from seeking to 
invalidate its intellectual property, or block sales of its products by alleging a breach of 
their intellectual property. Applications filed by the Group in respect of new patents and 
trademarks may also not be granted.

The Directors intend to defend the Group’s intellectual property vigorously through 
litigation and other means.

Infringement of third-
party patents and  
other intellectual 
property rights

Protection of 
trademarks

The Group’s products may infringe or may be alleged to infringe existing patents or 
patents that may be granted in the future, which may result in costly litigation and 
could result in the Group having to pay substantial damages or limit the Group’s ability 
to commercialise its products.

If the Group is sued for patent infringement, the Group would need to demonstrate that 
its products or methods either do not infringe the patent claims of the relevant patent 
or that the patent claims are invalid, and the Group may not be able to do this. If the 
Group is found to have infringed a third-party’s patent, the Group could be required 
to obtain a licence from such third party to continue developing and marketing its 
products and technology or the Group may elect to enter into such a licence in order 
to settle litigation or in order to resolve disputes prior to litigation. However, the Group 
may not be able to obtain any required licence on commercially reasonable terms or 
at all. Even if the Group is able to obtain a licence, it could be non-exclusive, thereby 
giving its competitors access to the same technologies licensed to the Group, and 
could require the Group to make substantial royalty payments. The Group could also 
be forced, including by court order, to cease commercialising the infringing technology 
or products.

A finding of infringement could prevent the Group from commercialising its products or 
force the Group to cease some of its business operations, which could materially harm 
its business. Claims that the Group has misappropriated the confidential information or 
trade secrets of third parties could have a similarly negative impact on its business.

The Group owns certain trademarks that are important to its business and competitive 
position. Third parties may infringe or misappropriate these rights by, for example, 
imitating the Group’s products, asserting rights in, or ownership of, the Group’s 
trademarks or other intellectual property rights or in trademarks that are similar 
to trademarks that the Group owns. In addition, the Group may fail to discover 
infringement of its intellectual property, and/or any steps taken or that will be taken 
by it may not be sufficient to protect its intellectual property rights or prevent others 
from seeking to invalidate its trademarks by alleging a breach of their trademarks and 
intellectual property.

Applications filed by the Group in respect of new trademarks may not be granted. 
In addition, some of the Group’s intellectual property may not be capable of being 
registered as belonging to the Group in all types of trademarks and all classes and the 
Group may, therefore, have difficulty protecting such intellectual property. Further, the 
Group may not be able to prevent others from using its brands (or other intellectual 
property that is not registered as belonging to the Group) at all or in a particular market.

If the Group is unable to protect its intellectual property rights against infringement 
or misappropriation, or if others assert rights in or seek to invalidate its intellectual 
property rights, this could have a material adverse effect on the Group’s business, 
financial condition, capital resources, results and/or future operations.

Customer concentration

During the period, a large percentage of Group revenue was made to a single 
customer, the DHSC.

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Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNovacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationBusiness 
Overview

Strategic 
Report

Our 
Governance

Financial 
Statements

Company 
Information

Principal Risks and  
Risk Management 

continued

Bad debtors

Foreign exchange rates

SARS-CoV-2  
Pandemic

The Group sells to companies of all sizes from small to medium-sized enterprises to 
blue-chip institutions, and operates in emerging markets, such as the Middle East, 
the Asia-Pacific region (including China and India), Africa (including Nigeria) and South 
America (including Venezuela), with its main customer during the period being the 
DHSC. Whilst the Group has, to date, successfully managed the risk of being paid for 
products and services sold into these companies and regions, as the Group grows and 
its customer base and distribution channels expands, there could be a higher risk that 
new customers do not pay in a timely manner and that bad debt increases.

The Group operates on a global basis and it has exposure to foreign exchange risk on 
purchases and sales that are denominated in currencies other than the Pound Sterling, 
Euro and US Dollar, which are the currencies of most of its receivables, expenditures, 
cash reserves and borrowings. The Pound Sterling, Euro and US Dollar exchange rates 
have fluctuated significantly in the past and may do so in the future. Consequently, 
revenue, expenditure, cash and borrowings may be higher or lower than anticipated by 
the Group.

In addition, the financial statements of the Group are denominated in Pounds Sterling 
which, therefore, give further exposure to foreign exchange rate fluctuations and may 
impact the financial results reported to its Shareholders, particularly as profits and losses 
arising from foreign currency transactions and on settlement of amounts receivable and 
payable in foreign currency are dealt with through the profit and loss statement.

The global pandemic continues to cause significant disruption and volatility to the entire 
diagnostics market. As clinical laboratories try to meet the demand for COVID-19 testing 
all other diagnostic testing has been impacted and reduced as testing capacity has been 
insufficient to meet all clinical demands. This balance of supply and demand is improving 
in some parts of the world but continues to be challenging for all testing service providers 
as the pandemic evolves in waves across the globe and as the specific requirements for 
testing changes with the evolution of new virus mutations and the need for near patient 
testing alongside central testing. This makes the diagnostics market as a whole and 
COVID-19 testing specifically very difficult to predict and so diagnostic manufacturers are 
unable to plan or forecast their business requirements with any degree of accuracy.

72
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Novacyt Group Annual Report and Accounts for the year ended 31 December 2020

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Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Financial
Statements

Statement of Directors’ responsibilities  
in respect of the annual report and  
financial statements.

The Directors are responsible for preparing the Annual Report and the financial 
statements in accordance with applicable law and regulations.

F
I
N
A
N
C
A
L
S

I

Company law requires the Directors to 
prepare Group and parent company 
financial statements for each financial 
year. Under that law, they are required to 
prepare the Group financial statements 
in accordance with International Financial 
Reporting Standards, as adopted by the 
EU, and applicable law, and have elected 
to prepare the parent company financial 
statements under French GAAP. 

Under company law the Directors must 
not approve the financial statements 
unless they are satisfied that they give a 
true and fair view of the state of affairs of 
the Group and parent company and of 
their profit or loss for that period. 

In preparing each of the Group and 
parent company financial statements, the 
Directors are required to: 

•  Select suitable accounting policies and 

then apply them consistently;

•  Make judgements and accounting 
estimates that are reasonable and 
prudent;

•  State whether they have been prepared 
in accordance with IFRSs as adopted 
by the EU; and 

•  Prepare the financial statement on 
the going concern basis unless it is 
inappropriate to presume that the 
group and the parent company will 
continue in business.

The Directors are responsible for keeping 
adequate accounting records that are 
sufficient to show and explain the parent 
company’s transactions and disclose 
with reasonable accuracy at any time the 
financial position of the parent company 
and enable them to ensure that the 

Group’s financial statements comply with 
the Companies Act 2006. They have 
general responsibility for taking such 
steps as are reasonably open to them to 
safeguard the assets of the group and 
to prevent and detect fraud and other 
irregularities. 

Under applicable law and regulations, 
the Directors are also responsible for 
preparing a Strategic Report, Directors’ 
Report, Directors’ Remuneration Report 
and Corporate Governance Statement 
that complies with that law and those 
regulations.

Responsibility statement 
of the Directors in respect 
of the annual financial 
report
We confirm that to the best of our 
knowledge:

•  The financial statements, prepared in 
accordance with the applicable set 
of accounting standards, give a true 
and fair view of the assets, liabilities, 
financial position and profit or loss of 
the Company and the undertakings 
included in the consolidation taken  
as a whole; and

•  The Strategic report includes a fair 
review of the development and 
performance of the business and 
the position of the Company and 
the undertakings included in the 
consolidation taken as a whole,  
together with a description of the 
principal risks and uncertainties that 
they face.

74

75

Statutory auditor’s report on the 
consolidated financial statements 

Statutory Auditor’s report on the consolidated financial statements
Year ended December 31, 2020

This is a translation into English of the statutory auditor’s report on the consolidated financial statements of the Company issued in 
French and it is provided solely for the convenience of English speaking users.

This statutory auditor’s report includes information required by European regulation and French law, such as information about the 
appointment of the statutory auditor or verification of the management report and other documents provided to shareholders.

This report should be read in conjunction with, and construed in accordance with, French law and professional auditing standards 
applicable in France.

To the NOVACYT Shareholders’ Meeting,

Opinion
In compliance with the engagement 
entrusted to us by your annual 
general meeting, we have audited the 
accompanying consolidated financial 
statements of NOVACYT for the year 
ended December 31 2020.

In our opinion, the consolidated financial 
statements give a true and fair view of the 
assets and liabilities and of the financial 
position of the Group as at December 31 
2020 and of the results of its operations 
for the year then ended in accordance 
with International Financial Reporting 
Standards as adopted by the European 
Union.

Basis for Opinion
Audit Framework

We conducted our audit in accordance 
with professional standards applicable 
in France. We believe that the audit 
evidence we have obtained is sufficient 
and appropriate to provide a basis for our 
opinion.

Our responsibilities under those standards 
are further described in the “Statutory 
Auditor’s Responsibilities for the Audit of 
the Consolidated Financial Statements” 
section of our report.

Independence

We conducted our audit engagement 
in compliance with independence 

requirements of the French Commercial 
Code (code de commerce) and the 
French Code of Ethics (code de 
déontologie) for statutory auditors for the 
period from January 1 2020 to the date of 
our report.

Observations

Without qualifying the opinion, we draw 
your attention to:

•  the “Change in presentation 

currency” note to the consolidated 
financial statements, setting out the 
methodology and the impact of the 
change in the presentation currency of 
the consolidated financial statements.

•  Note 50, Contingent liabilities, 

identifying an ongoing commercial 
dispute and disclosing the underlying 
assumptions and the potential 
impacts in the consolidated financial 
statements.

Justification of our assessments 
Due to the global crisis related to the 
Covid-19 pandemic, the financial 
statements of this period have been 
prepared and audited under specific 
conditions. Indeed, this crisis and the 
exceptional measures taken in the 
context of the state of sanitary emergency 
have had numerous consequences 
for companies, particularly on their 
operations and their financing, and 
have led to greater uncertainties on 

their future prospects. Those measures, 
such as travel restrictions and remote 
working, have also had an impact on the 
companies’ internal organization and the 
performance of the audits.

It is in this complex and evolving context 
that, in accordance with the requirements 
of Articles L. 823-9 and R. 823-7 of the 
French Commercial Code relating to 
the justification of our assessments, we 
inform you of the following assessments 
that, in our professional judgment, were 
of most significance in our audit of the 
consolidated financial statements of the 
current period.

These matters were addressed in the 
context of our audit of the consolidated 
financial statements as a whole, and in 
forming our opinion thereon. We do not 
provide a separate opinion on specific 
items of the consolidated financial 
statements.

Goodwill

Goodwill was subject to impairment tests 
according to the procedures described 
in the “Impairment testing” note to 
the consolidated financial statements. 
We reviewed the procedures used to 
implement these tests as well as the cash 
flow forecasts and assumptions used 
for this purpose, and we verified that the 
“Impairment testing” and “Goodwill” notes 
provided appropriate disclosures.

Specific verifications
We have also performed, in accordance 
with professional standards applicable in 
France, the specific verifications required 
by laws and regulations of the information 
presented in the Board of Directors’ 
management report.

We have no matters to report as to its fair 
presentation and its consistency with the 
consolidated financial statements.

Responsibilities of 
Management and Those 
Charged with Governance for 
the Consolidated Financial 
Statements
Management is responsible for the 
preparation and fair presentation of the 
consolidated financial statements in 
accordance with International Financial 
Reporting Standards as adopted by the 
European Union, and for such internal 
control as Management determines is 
necessary to enable the preparation of 
consolidated financial statements that are 
free from material misstatement, whether 
due to fraud or error.

In preparing the consolidated financial 
statements, Management is responsible 
for assessing the Company’s ability to 
continue as a going concern, disclosing, 
as applicable, matters related to going 
concern and using the going concern 
basis of accounting unless it is expected 
to liquidate the Company or to cease 
operations. 

The consolidated financial statements 
were approved by the Board of Directors.

Statutory Auditor’s 
Responsibilities for the Audit 
of the Consolidated Financial 
Statements
Our role is to issue a report on the 
consolidated financial statements. 
Our objective is to obtain reasonable 
assurance about whether the 
consolidated financial statements 
as a whole are free from material 
misstatement. Reasonable assurance 

is a high level of assurance, but is not 
a guarantee that an audit conducted in 
accordance with professional standards 
will always detect a material misstatement 
when it exists. Misstatements can arise 
from fraud or error and are considered 
material if, individually or in the aggregate, 
they could reasonably be expected to 
influence the economic decisions of 
users taken on the basis of these financial 
statements.

As specified in Article L. 823-10-1 of 
the French Commercial Code (code de 
commerce), our statutory audit does not 
include assurance on the viability of the 
Company or the quality of management of 
the affairs of the Company.

As part of an audit conducted in 
accordance with professional standards 
applicable in France, the statutory 
auditor exercises professional judgment 
throughout the audit and furthermore: 

•  Identifies and assesses the risks 
of material misstatement of the 
consolidated financial statements, 
whether due to fraud or error, designs 
and performs audit procedures 
responsive to those risks, and obtains 
audit evidence considered to be 
sufficient and appropriate to provide 
a basis for his opinion The risk of not 
detecting a material misstatement 
resulting from fraud is higher than for 
one resulting from error, as fraud may 
involve collusion, forgery, intentional 
omissions, misrepresentations, or the 
override of internal control;

•  Obtains an understanding of internal 
control relevant to the audit in order 
to design audit procedures that are 
appropriate in the circumstances, but 
not for the purpose of expressing an 
opinion on the effectiveness of the 
internal control;

•  Evaluates the appropriateness of 
accounting policies used and the 
reasonableness of accounting 
estimates and related disclosures 
made by management in the 
consolidated financial statements;

•  Assesses the appropriateness of 
management’s use of the going 
concern basis of accounting and, 
based on the audit evidence obtained, 
whether a material uncertainty exists 
related to events or conditions that 
may cast significant doubt on the 
Company’s ability to continue as a 
going concern. This assessment is 
based on the audit evidence obtained 
up to the date of his audit report. 
However, future events or conditions 
may cause the Company to cease to 
continue as a going concern. If the 
statutory auditor concludes that a 
material uncertainty exists, there is a 
requirement to draw attention in the 
audit report to the related disclosures 
in the consolidated financial statements 
or, if such disclosures are not provided 
or inadequate, to modify the opinion 
expressed therein;

•  Evaluates the overall presentation of 
the consolidated financial statements 
and assesses whether these 
statements represent the underlying 
transactions and events in a manner 
that achieves fair presentation.

•  Obtains sufficient appropriate audit 
evidence regarding the financial 
information of the entities or business 
activities within the Group to express 
an opinion on the consolidated 
financial statements. The statutory 
auditor is responsible for the direction, 
supervision and performance of the 
audit of the consolidated financial 
statements and for the opinion 
expressed on these consolidated 
financial statements. 

Paris-La Défense, June 21, 2021

The Statutory Auditor 
Deloitte & Associés 
Benoit Pimont

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Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationConsolidated statement of 
comprehensive income

for the years ended 31 December 2020 and 31 December 2019

Amounts in £‘000
Profit/(loss) after tax
Items that may be reclassified subsequently to profit or loss:
Translation reserves
Total comprehensive profit/(loss)
Comprehensive profit/(loss) attributable to:
Owners of the Company**

*  The comparative information for 2019 has been restated to reflect the change in presentation currency of the Group (see note 3). 

** There are no non-controlling interests. 

Year ended 
31 December 
2020
132,423 

Year ended 
31 December 
2019*

(5,749) 

290 
132,713 

(194) 
(5,943) 

132,713 

(5,943)

Consolidated income statement

for the years ended 31 December 2020 and 31 December 2019

Amounts in £'000
Continuing Operations
Revenue
Cost of sales
Gross profit
Sales, marketing and distribution expenses
Research and development expenses
General and administrative expenses
Governmental subsidies
Operating profit/(loss) before exceptional items
Other operating income
Other operating expenses
Operating profit/(loss) after exceptional items
Financial income
Financial expense
Profit/(loss) before tax
Tax (expense)/income
Profit/(loss) after tax from continuing operations
Loss from discontinued operations
Profit/(loss) after tax attributable to owners of the Company**
Profit/(loss) per share (£)
Diluted profit/(loss) per share (£)
Profit/(loss) per share from the continuing operations (£)
Diluted profit/(loss) per share from the continuing operations (£)
Loss per share from the discontinued operations (£)
Diluted loss per share from the discontinued operations (£)

Year 
ended 31 
December 
2020

Year ended 
31 December 
2019* 

Notes

5
7

8
9
10

11
11

12
12

13

41

14
14

277,204 
(65,704)
211,500 
(4,492) 
(1,630) 
(30,532) 
(3) 
174,843 
–

(7,402) 
167,441 
83 
(2,353) 
165,171 
(32,748) 
132,423
– 
132,423 
1.94
1.94
1.94
1.94
0.00
0.00

11,468 
(4,128) 
7,340 
(2,367) 
(395)
(5,669)
3 
(1,088) 
111 
(579) 
(1,556) 
228 
(2,098) 
(3,426) 
7 
(3,419) 
(2,330) 
(5,749) 
(0.13)
(0.13)
(0.08)
(0.08)
(0.05)
(0.05)

*  The comparative information for 2019 has been restated to reflect the change in presentation currency of the Group (see note 3). 
** There are no non-controlling interests.

The 2019 consolidated income statement is presented to reflect the impacts of the application of IFRS 5 relative to discontinued 
operations, by stating the NOVAprep activity on a single line “Loss from discontinued operations”.

78

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Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationStatement of financial position

for the years ended 31 December 2020, 31 December 2019 and 31 December 2018

Statement of changes in equity

for the years ended 31 December 2020 and 31 December 2019

Amounts in £‘000
Goodwill
Other intangible assets
Property, plant and equipment
Right of use assets
Non-current financial assets
Deferred tax assets
Other long-term assets
Total non-current assets
Inventories and work in progress
Trade and other receivables
Tax receivables
Prepayments and short-term deposits
Investments short-term
Cash and cash equivalents
Total current assets
Assets classified as held for sale
Total assets
Bank overdrafts and current portion of long-term borrowings
Lease liabilities short-term
Contingent consideration short-term
Provisions short-term
Trade and other liabilities
Tax liabilities
Other current liabilities
Total current liabilities
Liabilities directly associated with assets classified as held for sale
Net current assets/(liabilities)
Borrowings and convertible bond notes
Lease liabilities long-term
Contingent consideration long-term
Provisions long-term
Deferred tax liabilities
Other liabilities long-term
Total non-current liabilities
Total liabilities
Net assets
Share capital
Share premium account
Own shares
Other reserves
Equity reserve
Retained earnings/(losses)
Total equity – owners of the Company
Total equity

Notes
15
16
17
18
19
20
21

22
23

24

25

26
27
29
30
31
32
33

26
27
29
30
20
34

35
36

37
38
39

Year ended 
31 December 
2020
17,877 
4,255 
1,643 
2,259 
 138 
  3,023 
  96 
29,291 
29,888 
79,592 
– 
3,731 
9 
91,765 
204,985 
– 
234,276 
– 
414
1,022 
19,856 
36,784 
  15,116 
950 
74,142 
– 
130,843 
– 
1,964
  812 
242 
800 
5,606 
9,424 
83,566 
150,710 
4,053 
50,671 
(49) 
(2,036) 
1,155 
96,916 
150,710 
150,710 

Year ended 
31 December 
2019*
13,592 
3,683 
846 
2,125
195 
–
  183 
20,624 
2,083 
1,851 
3 
356 
8 
1,542 
5,843 
60 
26,527 
1,869 
229
– 
43 
3,920 
– 
505 
6,566 
–
(663) 
5,240 
2,012
– 
205 
42 
– 
7,499 
14,065 
12,462 
3,311 
46,999 
(141) 
(1,924) 
336 
(36,119) 
12,462 
12,462 

Year ended 
31 December 
2018*
14,548 
4,458 
1,074 
–
 203 
–
– 
20,283 
2,116 
3,517 
85 
218 
9 
1,021 
6,966 
2,068 
29,317 
2,809 
–
1,415 
90 
4,190 
– 
341 
8,845 
77 
112 
2,037 
–
– 
151 
48 
– 
2,236 
11,158 
18,159 
2,117 
47,207 
(144) 
(4,395) 
355 
(26,981) 
18,159 
18,159 

* The comparative information for 2019 and 2018 has been restated to reflect the change in presentation currency of the Group (see note 3).

Notes

Share 
capital

Share 
premium

Own 
shares

Equity 
reserves

2,117 47,207
–
–

–
–

(144)
–
–

–
–

–
1,194

–
(158)

–
(50)

–
–

3
–

3,311 46,999
–
–

–
–

(141)
–
–

35,36

–
567

–
2,011

–
–

–

–

92

355
–
–

–
–

–
(19)

336
–
–

–
–

–

35,36

175

1,661

–

819

Other group reserves 

Acquisition 
of the 
shares of 
Primerdesign

Translation 
reserve

OCI on 
retirement 
benefits

Retained 
earnings 

Total 
equity

Total

(2,407)
–
–

(1,980)
2,471
–

(8)
–
–

(4,395) (26,981) 18,159
2,471
2,471
(5,749)
–

–
(5,749)

–
–

–
–

(2,407)
–
–

–
–

–

–

2,471
–

–
–

491
(112)
–

(112)
–

–

–

–
–

–
–

2,471
–

(5,749)
–

(3,278)
(158)

–
–

–
(3,389)

3
(2,264)

(8)
–
–

(1,924) (36,119) 12,462
–
(112)
– 132,423 132,423

(112)

–
–

–

–

(112) 132,423 132,311
2,578

–

–

–

–

–

92

612

3,267

4,053 50,671

(49)

1,155

(2,407)

379

(8)

(2,036) 96,916 150,710

Amounts in £‘000
Balance at  
1 January 2019*
Translation differences
Loss for the period
Total comprehensive 
income/(loss) for  
the period
Issue of share capital
Own shares acquired/
sold in the period
Other changes
Balance at  
31 December 2019*
Translation differences
Profit for the period
Total comprehensive 
income/(loss) for the 
period
Issue of share capital
Own shares acquired/
sold in the period
Conversion of 
warrants and debts
Balance at  
31 December 2020

* The comparative information for 2019 has been restated to reflect the change in presentation currency of the Group (see note 3).

The line “Conversion of warrants and debts” is showing in the column “Share capital”; the amount of the share capital increase that 
was completed by conversion of the Vatel debt and had no impact on the cash situation of the Group (see note 35).

The line “Conversion of warrants and debts” is showing in the column “Share premium”; the amount of the share premium increase 
that occurred by conversion of the Vatel debt and had no impact on the cash situation of the Group (see note 35).

The line “Conversion of warrants and debts” is showing in the column “Equity reserve”; the IFRS impact on the Group equity of the 
conversion of the various warrants outstanding at 31 December 2020 (see note 14).

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Statement of cash flows

for the years ended 31 December 2020 and 31 December 2019

Notes to the annual accounts

for the years ended 31 December 2020 and 31 December 2019

Amounts in £‘000
Net cash from (used in) operating activities
Investing activities
Proceeds from disposal of property, plant and equipment
Purchases of patents and trademarks
Purchases of property, plant and equipment
Variation of deposits
Acquisition of subsidiary net of cash acquired
Proceeds from the sale of businesses
Net cash used in investing activities
Investing cash flows from discontinued activities
Investing cash flows from continuing operations
Financing activities
Repayments of borrowings
Proceeds on issue of borrowings and bond notes
Repayment of lease liabilities
Proceeds from issue of shares
Disposal (purchase) of own shares – net
Repayment of other short-term financing facilities
Proceeds from other short-term financing facilities
Negma phantom awards settlement
Interest paid
Net cash (used in) from financing activities
Financing cash flows from discontinued activities
Financing cash flows from continuing operations
Net increase in cash and cash equivalents
Cash and cash equivalents at beginning of year
Effect of foreign exchange rate changes
Cash and cash equivalents at end of year

Year ended 
31 December 
2020
102,976

Year ended 
31 December 
2019*
(941) 

Notes
42

–
(168)
(1,013)
74
(6,858)
–
(7,965)
–
(7,965)

(4,592)
–
(303)
2,577
92
(720)
–
(439)
(1,655)
(5,040)
–
(5,040)
89,971
1,542
252
91,765

24
(99)
(105) 
–
(1,186)
319
(1,047)
138
(1,185)

(2,756)
5,922
(183)
(158)
4
(93)
677
–
(918)
2,495
–
2,495
507
1,021
14
1,542

1. APPLICABLE ACCOUNTING STANDARDS
The Novacyt Group is an international diagnostics business generating an increasing portfolio of invitro and molecular diagnostic 
tests. Its core strengths lie in diagnostics product development, commercialisation, contract design and manufacturing. The Group’s 
lead business units comprise of Primerdesign and Lab21 Products, supplying an extensive range of high-quality assays and reagents 
worldwide. The Group directly serves microbiology, haematology and serology markets as do its global partners, which include major 
corporates. Its registered office is located at 13 Avenue Morane Saulnier, 78140 Vélizy Villacoublay.

The financial information contained in this report comprises the consolidated financial statements of the Company and its subsidiaries 
(hereinafter referred to collectively as the “Group”). They are prepared and presented in £’000s of Great British Pounds “GBP”.

The 2020 consolidated financial statements were approved by the Board of Directors on 21 June 2021.

2. ADOPTION OF NEW STANDARDS AND AMENDMENTS TO EXISTING 
STANDARDS 
•  Standards, interpretations and amendments to standards with mandatory application for the period beginning on or after 1 

January 2020 had no material impact on Novacyt’s consolidated financial statements at 31 December 2020. These are mainly:

 − Amendments to IFRS 3 “Business Combinations – Definition of a Business”;

 − Amendments to IAS 1 and IAS 8 “Definition of Material”;

 − Amendments to References to the Conceptual Framework in IFRS Standards;

 − Amendments to IFRS 9 and IFRS 7 – “Interest Rate Benchmark Reform – Phase 1”;

 − IFRS IC interpretation relating to the assessment of non-cancellable periods of leases and the amortisation period of leasehold 

improvements;

 − Amendment to IFRS 16 “Leases – COVID-19-related Rent Concessions”, approved by the European Union on 12 October 

2020. This amendment has no impact on the consolidated financial statements at 31 December 2020.

The Group has not elected to take early adoption of any standards or interpretations not mandatorily applicable in 2020.

The texts adopted by the European Union are available on the website of the European Commission. 

The Group has not applied the following IFRSs that have been issued but are not yet effective:

 − IFRS 17 “Insurance Contracts”, applicable from 1 January 2023. The standard will have no impact on the Group accounts.

 − IFRS 10 and IAS 28 (amendments) “Sale or Contribution of Assets between an Investor and its Associate or Joint Venture”. The 

standard will have no impact on the Group accounts.

* The comparative information for 2019 has been restated to reflect the change in presentation currency of the Group (see note 3).

 − Amendments to IAS 1 “Classification of Liabilities as Current or Non-current”, applicable from 1 January 2022. The Group does 

not expect any significant impact of the standard on the annual accounts.

 − Amendments to IFRS 3 ”Reference to the Conceptual Framework”, applicable from 1 January 2022. The Group does not 

expect any significant impact of the standard on the annual accounts.

 − Amendments to IAS 16 “Property, Plant and Equipment – Proceeds before Intended Use”, applicable from 1 January 2022. The 

standard will have no impact on the Group accounts.

 − Amendments to IAS 37 “Onerous Contracts – Cost of Fulfilling a Contract”, applicable from 1 January 2022. The Group does 

not expect any significant impact of the standard on the annual accounts.

 − Annual Improvements to IFRS Standards 2018–2020 Cycle – Amendments to IFRS 1 “First-time Adoption of International 

Financial Reporting Standards”, IFRS 9 “Financial Instruments”, IFRS 16 “Leases”, and IAS 41 “Agriculture”, applicable from 1 
January 2022. The Group does not expect any significant impact of the standard on the annual accounts.

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The financial statements have been prepared in accordance with International Financial Reporting Standards (“IFRSs”). The financial 
statements have also been prepared in accordance with IFRSs adopted by the European Union and therefore the Group financial 
statements comply with Article 4 of the EU IAS Regulation.

The financial information has been prepared on the historical cost basis except in respect of those financial instruments that have 
been measured at fair value. Historical cost is generally based on the fair value of the consideration given in exchange for the goods 
and services.

Fair value is the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market 
participants at the measurement date, regardless of whether that price is directly observable or estimated using another valuation 
technique. In estimating the fair value of an asset or a liability, the Group takes into account the characteristics of the asset or liability 
if market participants would take those characteristics into account when pricing the asset or liability at the measurement date. Fair 
value for measurement and/or disclosure purposes in the financial information is determined on such a basis, except for leasing 
transactions that are within the scope of IFRS 16, and measurements that have some similarities to fair value but are not fair value, 
such as net realisable value in IAS 2 or value in use in IAS 36.

The areas where assumptions and estimates are material in relation to the financial information are the measurement of goodwill 
resulting from the Group’s acquisition of IT-IS International (see note 15), the carrying amounts and useful lives of the other intangible 
assets (see note 16), deferred taxes (see note 20), trade receivables (see note 23) and provisions for risks and other provisions 
related to the operating activities (see note 30).

The accounting policies set out below have been applied consistently to all periods presented in the financial information.

Change of presentation currency
The Group has opted to change its presentation currency to GBP to better reflect the Group’s trading activities, which are mainly 
conducted in GBP. 

Following this change in accounting policy, the comparative consolidated financial statements are presented in GBP. Consolidation 
translation differences were reset to zero as of 1 January 2014, the date of creation of the consolidated Group. The cumulative 
translation differences on consolidation are presented as if the Group had used the GBP as its presentation currency for its 
consolidated financial statements since that date, 1 January 2014.

The functional currency of the Parent Company, Novacyt SA, remains the Euro. Translation differences arising from the Parent 
Company are presented in “other reserves”.

Capital, premium and reserves
Translation differences
Net equity

(a) Translation at the €/£ closing rate of 0.85391.

Year ended 31 
December 2019  
in €‘000 

14,941
(347)
14,594

Year ended 31 
December 2019  
translated to 
£‘000  
(a) 
12,758
(296)
12,462

Adjustments in 
£‘000  
(b)
(838)
838
–

Year ended 31 
December 2019 
restated in £‘000 

11,971
491
12,462

(b) Differences between the historical rates and the closing rate of £0.85391 for €1, including the translation differences of the French  

holding company in the amount of £674,000 reclassified to “other reserves”.

3. SUMMARY OF ACCOUNTING POLICIES APPLIED BY THE GROUP continued
Basis of consolidation
The financial information includes all companies under control. The Group does not exercise joint control or have significant influence 
over other companies. Subsidiaries are consolidated from the date on which the Group obtains effective control.

Controlled companies are consolidated by the full consolidation method with recognition of non-controlling interests. Under IFRS 10, 
an investor controls an investee when it is exposed, or has rights, to variable returns from its involvement with the investee and has 
the ability to affect those returns through its power over the investee.

When the Group has less than a majority of the voting rights of an investee, it considers that it has power over the investee when the 
voting rights are sufficient to give it the practical ability to direct the relevant activities of the investee unilaterally. The Group considers 
all relevant facts and circumstances in assessing whether or not the Group’s voting rights in an investee are sufficient to give it power, 
including: 

•  the size of the Company’s holding of voting rights relative to the size and dispersion of holdings of the other vote holders; 

•  potential voting rights held by the Company, other vote holders or other parties; 

•  rights arising from other contractual arrangements; and 

•  any additional facts and circumstances that indicate that the Company has, or does not have, the current ability to direct the 
relevant activities at the time that decisions need to be made, including voting patterns at previous Shareholders’ meetings. 

Consolidation of a subsidiary begins when the Group obtains control over the subsidiary and ceases when the Group losses control 
of the subsidiary. Specifically, the results of subsidiaries acquired or disposed of during the year are included in the consolidated 
income statement from the date the Group gains control until the date when the Group ceases to control the subsidiary.

Profit or loss and each component of other comprehensive income are attributed to the owners of the Group and to the non-
controlling interests. Total comprehensive income of the subsidiaries is attributed to the owners of the Group and to the non-
controlling interests even if this results in the non-controlling interests having a deficit balance. 

Where necessary, adjustments are made to the financial statements of subsidiaries to bring the accounting policies used into line with 
the Group’s accounting policies. 

All intragroup assets and liabilities, equity, income, expenses and cash flows relating to transactions between the members of the 
Group are eliminated on consolidation. The Group’s scope of consolidation included the following companies, all fully consolidated 
when included in the scope.

Companies
Biotec Laboratories Ltd
IT-IS International Ltd
Lab21 Healthcare Ltd
Lab21 Ltd
Microgen Bioproducts Ltd
Novacyt SA
Novacyt Asia Ltd
Novacyt China Ltd
Novacyt UK Holdings Ltd
Primerdesign Ltd

Legend: 

FC: Full consolidation 

At 31 December 2020

At 31 December 2019

At 31 December 2018

 Interest 
percentage 
100% 
100% 
100% 
0% 
100% 
100% 
100% 
100% 
100% 
100% 

Consolidation 
method
FC
FC
FC
–
FC
FC
FC
FC
FC
FC

 Interest 
percentage 

100% 
0% 
100% 
0%
100% 
100% 
100% 
100% 
100% 
100% 

Consolidation 
method
FC
–
FC
–
FC
FC
FC
FC
–
FC

 Interest 
percentage 
100% 
0% 
100% 
100% 
100% 
100% 
100% 
100% 
0% 
100% 

Consolidation 
method
FC
–
FC
FC
FC
FC
FC
FC
–
FC

On 15 October 2020, Novacyt UK Holdings Limited purchased the entire share capital of IT-IS International Limited.

84

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3. SUMMARY OF ACCOUNTING POLICIES APPLIED BY THE GROUP continued
Consolidation methods
The consolidated historical financial information is prepared using uniform accounting policies for transactions and other similar 
events in similar circumstances.

Elimination of intercompany transactions

The intercompany balances arising from transactions between consolidated companies, as well as the transactions themselves, 
including income, expenses and dividends, are eliminated.

Translation of accounts denominated in foreign currency

The historical financial information is presented in £’000 GBP. The financial statements of companies whose functional currency is not 
GBP are translated into GBP as follows:

•  Items in the statement of financial position are translated at the closing exchange rate, excluding equity items, which are stated at 

historical rates; and

•  Transactions in the income statement and statement of cash flows are translated at the average annual exchange rate.

Translation differences on earnings and equity are recognised directly in other comprehensive income under “Translation reserves” for 
the portion attributable to the Group. On disposal of a foreign company, the translation differences relating thereto and recognised in 
other comprehensive income are reclassified to profit or loss.

3. SUMMARY OF ACCOUNTING POLICIES APPLIED BY THE GROUP continued
Pursuant to IFRS 3R, the Group applies the following principles: 

•  Transaction costs are recognised immediately as operating expenses when incurred;

•  Any purchase price adjustment of an asset or a liability assumed is estimated at fair value at the acquisition date, and the 
initial assessment may only subsequently be adjusted against goodwill in the event of new information related to facts and 
circumstances existing at the acquisition date if this assessment occurs within the 12-month allocation period after the acquisition 
date. Any adjustment of the financial liability recognised in respect of an additional price subsequent to the intervening period or 
not meeting these criteria is recognised in the Group’s comprehensive income;

•  Any negative goodwill arising on acquisition is immediately recognised as income; and

•  For step acquisitions, the achievement of control triggers the remeasurement at fair value of the interest previously held by the 

Group in profit or loss. Loss of control results in the remeasurement of the possible residual interest at fair value in the same way.

For companies acquired during the year, only the results for the period following the acquisition date are included in the consolidated 
income statement. For the financial year 2020, this applies to IT-IS International Ltd, which was acquired on the 15 October 2020.

Measurement of goodwill

Goodwill is broken down by cash-generating unit (“CGU”) or group of CGUs, depending on the level at which goodwill is monitored 
for management purposes. In accordance with IAS 36, none of the CGUs or groups of CGUs defined by the Group are greater in 
size than an operating segment.

Exchange differences arising from intragroup balances are recognised as exchange losses or gains in the consolidated income 
statement. 

Impairment testing

Going concern
The Directors have, at the time of approving the financial statements, a reasonable expectation that the Group has adequate 
resources to continue in operational existence for the foreseeable future. Thus, they adopt the going concern basis of accounting in 
preparing the financial statements.

The going concern model covers the period up to and including June 2022. In making this assessment, the Directors have 
considered the following elements: 

•  The working capital requirements of the business;

•  A positive cash balance at 31 December 2020 of £91,765,000;

•  Payment of the second tranche of the Long-Term Incentive Plan (“LTIP”) that commenced in November 2017 and concluded in 

November 2020;

•  Payment of the first earn-out milestone related to the IT-IS International acquisition; and

•  Management’s confidence in settling the outstanding commercial dispute as per note 50.

In the event the current dispute is fully settled in favour of the counterparty, the forecast prepared by the Group shows that it is able to 
cover its cash needs during the financial year 2021 and until June 2022 without the raising of any banking or other financing facility. 

Business combinations and measurement of goodwill
Business combinations

Business combinations are accounted for using the purchase method (see IFRS 3R).

Each time it acquires a company or group of companies constituting a business, the Group identifies and measures the assets 
acquired and liabilities assumed, most of which are carried at fair value. The difference between the fair value of the consideration 
transferred, including the recognised amount of any non-controlling interest in the acquiree and the net amount recognised in respect 
of the identifiable assets acquired and liabilities assumed measured at fair value, is recognised as goodwill.

Goodwill is not amortised, but is subject to impairment testing when there is an indication of loss of value, and at least once a year at 
the reporting date.

Such testing consists of comparing the carrying amount of an asset to its recoverable amount. The recoverable amount of an asset, 
a CGU or a group of CGUs is the greater of its fair value less costs to sell and its value in use. Fair value less costs to sell is the 
amount obtainable from the sale of an asset, a CGU or a group of CGUs in an arm’s length transaction between well-informed, willing 
parties, less the costs of disposal. Value in use is the present value of future cash flows expected to arise from an asset, a CGU or a 
group of CGUs.

It is not always necessary to determine both the fair value of an asset less costs to sell and its value in use. If either of these amounts 
exceeds the carrying amount of the asset, the asset is not impaired and it is not necessary to estimate the other amount.

Intangible fixed assets
Customer relationships

In accordance with IFRS 3, the Group’s acquisition of Primerdesign, the Omega Infectious Diseases business and IT-IS International 
Ltd resulted in the recognition of the value of the acquired customer base on the statement of financial position. The value of these 
assets was determined by discounting the additional margin generated by customers after remuneration of the contributing assets.

Customer relationships will be amortised on a straight-line basis over nine years, unless it is deemed to be impaired.

Trademark

The acquisition price of Primerdesign, the Omega Infectious Diseases business and IT-IS International Ltd by the Group has led to 
the recognition of a number of trademarks. The value of these assets has been determined by discounting the cash flows that could 
be generated by licensing the trademark, estimated as a percentage of revenue derived from information available on comparable 
assets.

All trademarks are amortised on a straight-line basis over nine years, unless it is deemed to be impaired.

Other intangible assets

Intangible assets include licences and patents recognised at cost and amortised over useful lives of between 7 and 20 years.

86

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Property, plant and equipment
Items of property, plant and equipment are recognised at their acquisition cost (purchase price plus incidental expenses and 
acquisition costs).

Depreciation and amortisation
Property, plant and equipment and intangible assets are depreciated or amortised on a straight-line basis, with major components 
identified separately where appropriate, based on the following estimated useful lives:

•  Leasehold improvements: 

Straight-line basis – 2 to 15 years

•  Trademarks: 

Straight-line basis – 9 years

•  Customer relationships: 

Straight-line basis – 9 years

•  Plant and machinery: 

Straight-line basis – 3 to 6 years

•  General fittings, improvements: 

Straight-line basis – 3 to 5 years

•  Transport equipment: 

•  Office equipment: 

Straight-line basis – 5 years

Straight-line basis – 3 years

•  Computer equipment: 

Straight-line basis – 2 to 3 years

Any leased buildings, equipment or other leases that fall under the scope of IFRS 16 have been capitalised as a right-of-use asset 
and will be depreciated on a straight-line basis over the term of the lease.

The depreciation or amortisation of property, plant and equipment begins when they are ready for use and ceases at their disposal, 
scrapping or reclassification as assets held for sale in accordance with IFRS 5.

Given the nature of its assets, the Group does not recognise residual value on the items of property, plant and equipment it uses.

Depreciation and amortisation methods and useful lives are reviewed at each reporting date and revised prospectively if necessary.

Asset impairment 
Depreciable and non-depreciable assets are subject to impairment testing when indications of loss of value are identified. In 
assessing whether there is any indication that an asset may be impaired, the Group considers the following external and internal 
indicators:

External indicators:

•  Drop in the market value of the asset (to a greater extent than would be expected solely from the passage of time or the normal 

use of the asset);

•  Significant changes with an adverse effect on the entity, either having taken place during the period or expected to occur in the 
near future, in the technical, economic or legal environment in which the Group operates or in which the asset is used; and

•  Increases in market interest rates or other market rates of return during the year when it is likely that such increases will 

significantly reduce the market value and/or value in use of the asset.

Internal indicators:

•  Existence of indication of obsolescence or physical damage of an asset unforeseen in the depreciation or amortisation schedule;

•  Significant changes in the way the asset is used;

•  Weaker-than-expected performance by the asset; and

•  Significant reduction in the level of cash flow generated by the asset.

If there is an indication of impairment, the recoverable amount of the asset is compared with its carrying amount. The recoverable 
amount is the greater of fair value less costs to sell and value in use. Value in use is the present value of future cash flows expected to 
flow from an asset over its estimated useful life.

3. SUMMARY OF ACCOUNTING POLICIES APPLIED BY THE GROUP continued
The carrying amount of an asset is its gross value less accumulated depreciation, for depreciable property, plant and equipment, and 
impairment losses.

In the event of loss of value, an impairment charge is recognised in profit or loss. Impairment is reversed in the event of a change 
in the estimate of the recoverable value or if indications of loss of value disappear. Impairment is recognised under “Depreciation, 
amortisation and provisions for impairment of property, plant and equipment and intangible assets” in the income statement.

Intangible assets not subject to amortisation are tested for impairment at least once a year.

Leases 
The Group assesses whether a contract is or contains a lease, at inception of the contract. The Group recognises a right-of-use 
asset and a lease liability at lease commencement for all lease arrangements in which it is the lessee, except for short-term leases 
and leases of low-value assets.

•  The right-of-use asset is initially measured at the corresponding lease liability, lease payments made at or before the 

commencement day, less any lease incentives received and any initial direct costs and subsequently measured at cost less 
accumulated depreciation and impairment losses, adjusted for any remeasurement of the lease liability.

•  The lease liability is initially measured at the present value of the future lease payments discounted using the discount rate implicit 

in the lease (or if that rate cannot be readily determined, the lessee’s incremental borrowing rate). Subsequently, the lease liability is 
adjusted for interest and lease payments, as well as the impact of lease modifications, amongst others.

Inventories
Inventories are carried at the lesser of their acquisition cost and their recoverable amount. The acquisition cost of inventories includes 
materials and supplies, and, where applicable, personnel expenses incurred in transforming inventories into their current state. It 
is calculated using the weighted average cost method. The recoverable amount represents the estimated selling price less any 
marketing, sales and distribution expenses.

The gross value of goods and supplies includes the purchase price and incidental expenses.

A provision for impairment, equal to the difference between the gross value determined in accordance with the above terms and the 
current market price or the realisable value less any proportional selling costs, is recognised when the gross value is greater than the 
other stated item.

Trade receivables
The Group has an established credit policy under which the credit status of each new customer is reviewed before credit is 
advanced, including external credit evaluations where possible. Credit limits are established for all significant or high-risk customers, 
which represent the maximum amount permitted to be outstanding without requiring additional approval from the appropriate level 
of senior management. Outstanding debts are continually monitored by each division. Credit limits are reviewed on a regular basis, 
and at least annually. Customers that fail to meet the Group’s benchmark creditworthiness may only transact with the Group on a 
prepayment basis.

Trade receivables are recorded initially at fair value and subsequently measured at amortised cost. This generally results in their 
recognition at nominal value less an allowance for any doubtful debts. Trade receivables in foreign currency are transacted in 
their local currency and subsequently revalued at the end of each reporting period, with any foreign exchange differences being 
recognised in the income statement as an income/expense. 

The allowance for doubtful debts is recognised based on management’s expectation of losses without regard to whether an 
impairment trigger happened or not (an “expected credit loss” model). Through implementation of IFRS 9, the Group concluded that 
no real historical default rate could be determined due a low level of historical write offs across the business. The Group therefore 
recognises an allowance for doubtful debts on the basis of invoice ageing. Once an invoice is overdue from its due date, based on 
agreed upon credit terms by more than 90 days, that this invoice is then more likely to default than those invoices operating within 90 
days of their due date. As such, these invoices will be provided for in full as part of an expected credit loss model.

The recoverable amount of assets that do not generate independent cash flows is determined by that of the CGU to which it 
belongs; a CGU being the smallest homogeneous group of identifiable assets generating cash flows that are largely independent of 
other assets or groups of assets.

Trade receivables are written off when there is no reasonable expectation of recovery. Indicators that there may be no reasonable 
expectation of recovery may include the failure of the debtor to engage in a payment plan, and failure to make contractual payments 
within 365 days of the original due date.

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Cash and cash equivalents
Cash equivalents are held to meet short-term cash commitments rather than for investment or other purposes. For an investment 
to qualify as a cash equivalent, it must be readily convertible into a known amount of cash and be subject to an insignificant risk 
of change in value. Cash and cash equivalents comprise cash funds, current bank accounts and marketable securities (cash 
Undertakings for Collective Investment in Transferable Securities (“UCITS”), negotiable debt securities, etc.) that can be liquidated or 
sold within a very short time (generally with original maturities of three months or less) and which have a negligible risk of change in 
value. All such items are measured at fair value, with any adjustments recognised in profit or loss.

Financial liabilities
Borrowings are initially recognised at fair value. They are subsequently accounted for using the amortised cost method, based on 
the effective interest rate. Under this principle, any arranging costs are carried in the financial position item relating to the relevant 
borrowings and amortised in financial expense over the life of the loan.

Compound financial instruments 

Some financial instruments contain both a liability and an equity component. This is notably the case of the convertible bonds 
with warrants attached (Obligations Convertibles en Actions avec Bons de Souscription d’Actions (“OCABSAs”)), which are bonds 
convertible into shares with warrants. The various components of these instruments are accounted for and presented separately 
according to their substance, as defined in IAS 32 “Financial Instruments: Disclosure and Presentation”. The amortised cost is 
calculated on the basis of the liability only, once the embedded derivatives have been separated.

Primerdesign contingent consideration

The Group negotiated a contingent consideration for the acquisition of the Primerdesign securities with its former Shareholders, 
subject to the achievement of a revenue target. The final payment was made in November 2019.

3. SUMMARY OF ACCOUNTING POLICIES APPLIED BY THE GROUP continued
Provisions
In accordance with IAS 37 “Provisions, Contingent Liabilities and Contingent Assets”, a provision is recognised when the Group has 
a current obligation as of the reporting date in respect of a third party and it is probable or certain that there will be an outflow of 
resources to this third party, without at least equivalent consideration from the said third party. Provisions for risks and charges cover 
the amount corresponding to the best estimate of the future outflow of resources required to settle the obligation.

The provisions are for the restoration of leased premises, an industrial relations litigation, a long-term management incentive plan and 
product warranties.

Long-Term Incentive Plan
Novacyt granted to certain employees shares under a long-term management incentive plan adopted on 1 November 2017. The 
exercise price is set at the share price on the grant date and the options will be settled in cash. The options fully vested on the third 
anniversary of the grant date, 1 November 2020. The payment expenses are calculated under IFRS 2 “Share-Based Payments”. 
The accounting charge has been spread across the vesting period to reflect the services received and a liability recognised on the 
statement of financial position.

Discontinued operations and assets held for sale
Discontinued operations and assets held for sale are restated in accordance with IFRS 5. 

On the 18 July 2019, Novacyt disposed of Lab 21 Ltd, and on the 24 December 2019, Novacyt disposed of NOVAprep and, as a 
result, are presenting its financial results in accordance with the IFRS 5 accounting rule on discontinued operations. 

As a result, all revenues and charges generated by NOVAprep are presented on a single line, below the net result.

As per IFRS 5, we have presented discontinued operations as follows:

In accordance with IFRS 9, the financial liability has been remeasured at its fair value as of the balance sheet date. 

In the consolidated income statement and consolidated statement of comprehensive income, a single amount comprising the total of:

Omega Infectious Diseases contingent consideration

The Group negotiated a contingent consideration via the asset purchase agreement for the Omega Infectious Diseases business, 
subject to the achievement of certain deliverables. One of the milestones was paid in 2019, but the other milestone has not, and will 
not, be achieved.

In accordance with IFRS 9, the financial liability has been remeasured at its fair value as of the balance sheet date. 

IT-IS International Ltd contingent consideration

The Group negotiated a contingent consideration for the acquisition of the IT-IS International securities with its former Shareholders, 
subject to the achievement of a production volume target.

In accordance with IFRS 9, the financial liability has been remeasured at its fair value as of the balance sheet date. 

Trade payables

Trade payables are obligations to provide cash or other financial assets. They are recognised in the balance sheet when the Group 
becomes a party to a transaction generating liabilities of this nature. Trade and other payables are recognised in the balance sheet 
at fair value on initial recognition, except if settlement is to occur more than 12 months after recognition. In such cases, they are 
measured using the amortised cost method. The use of the effective interest rate method will result in the recognition of a financial 
expense in the income statement. Trade and other payables are eliminated from the balance sheet when the corresponding 
obligation is extinguished.

Trade payables have not been discounted, because the effect of doing so would be immaterial.

•  The post-tax profit or loss of the discontinued operation;

•  The post-tax gain or loss recognised on the measurement to fair value less costs to sell; and

•  The post-tax gain or loss recognised on the disposal of assets or the disposal group making up the discontinued operation.

The analysis of the single amount is presented in note 41.

In the statement of cash flows, the net cash flow attributable to the operating, investing and financing activities of discontinued 
operations have been disclosed separately.

In the statement of financial position, the assets and liabilities of a disposal group (Lab21 Ltd and NOVAprep) have been presented 
separately from other assets. The same applies for liabilities of a disposal group classified as held for sale.

Consolidated revenue
IFRS 15 “Revenue from Contracts with Customers” establishes a principles-based approach to recognising revenue only when 
performance obligations are satisfied, and control of the related goods or services is transferred. It addresses items such as the 
nature, amount, timing and uncertainty of revenue, and cash flows arising from contracts with customers. IFRS 15 replaces IAS 18 
“Revenue” and other related requirements. IFRS 15 applies a five-step approach to the timing of revenue recognition and applies to 
all contracts with customers except those in the scope of other standards. 

•  Step 1 – Identify the contract(s) with a customer 

•  Step 2 – Identify the performance obligations in the contract 

•  Step 3 – Determine the transaction price 

•  Step 4 – Allocate the transaction price to the performance obligations in the contract 

•  Step 5 – Recognise revenue when (or as) the entity satisfies a performance obligation. The Group principally satisfies its 

performance obligations at a point in time and the amounts of revenue recognised relating to performance obligations satisfied 
over time are not significant. Therefore, the accounting for revenue under IFRS 15 does not represent a substantive change for 
recognising revenue from sales to customers.

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The Group’s revenue recognition processes are generally straightforward, with recognition of revenue at the point of sale and 
little significant judgement required in determining the timing of transfer of control. Given that, the Group principally satisfies its 
performance obligations at a point in time and the amounts of revenue recognised relating to performance obligations satisfied over 
time are not significant.

Some contracts with customers contain a limited assurance warranty that is accounted for under IAS 37 (see provisions accounting 
policy). If a repair or replacement is not possible under the assurance warranty, a full refund of the product price may be given. The 
potential refund liability represents variable consideration. 

Under IFRS 15.53, the Group can use either:

•  The expected value (sum of probability weighted amounts); or

•  The most likely amount (generally used when the outcomes are binary).

The method used is not a policy choice. Management use the method that it expects will best predict the amount of consideration 
based on the terms of the contract. The method is applied consistently throughout the contract. Variable revenue is constrained if 
appropriate. IFRS 15 requires that revenue is only included to the extent that it is highly probable that there will not be a significant 
reversal in future periods. 

In making this assessment, management have considered the following factors (which are not exclusive):

•  If the amount of consideration is highly susceptible to factors outside the Group’s influence;

•  Whether the uncertainty about the amount of consideration is not expected to be resolved for a long period of time;

•  The Group’s experience (or other evidence) with similar types of contract;

•  The Group has a practice of either offering a broad range of price concessions or changing the payment terms and conditions of 

similar contracts in similar circumstances; and

•  The contract has a large number and broad range of possible consideration amounts.

The decision as to whether revenue should be constrained is considered to be a significant judgement as the term ‘highly probable’ 
is not defined in IFRS 15, management consider highly probable to be significantly more likely than probable.

The activity of NOVAprep

All the revenues generated by the NOVAprep activity were reclassified on the line “Loss from discontinued operations”. As a result, 
NOVAprep no longer contributes to the consolidated revenues of the Group. This business was sold on 24 December 2019.

The activity of Lab21 Products

Lab21 Limited provided laboratory-based diagnostic services. Revenue was recognised when the service was rendered (diagnosis 
made). This business was sold on 18 July 2019.

Lab21 Healthcare Ltd and Microgen Bioproducts Ltd is a developer, manufacturer and distributor of a large range of protein-based 
infectious disease IVD products. 

Revenue is recognised upon delivery of products sold and, where appropriate, after formal customer acceptance.

The activity of Primerdesign 

Primerdesign is a designer, manufacturer and marketer of molecular ‘real-time’ qPCR testing devices and reagents in the areas of 
infectious diseases. 

Revenue is recognised upon delivery of products sold and, where appropriate, after formal customer acceptance.

The activity of IT-IS International

IT-IS International is a UK based diagnostic instrument development and manufacturing company specialising in the development of 
PCR devices for the life sciences and food testing industry.

Revenue is recognised upon delivery of products sold and, where appropriate, after formal customer acceptance.

3. SUMMARY OF ACCOUNTING POLICIES APPLIED BY THE GROUP continued
Taxation
The tax expense represents the sum of the tax currently payable and deferred tax.

Current tax

The tax currently payable is based on taxable profit for the year. Taxable profit differs from net profit as reported in profit or loss 
because it excludes items of income or expense that are taxable or deductible in other years, and it further excludes items that are 
never taxable or deductible. The Group’s liability for current tax is calculated using tax rates that have been enacted or substantively 
enacted by the end of the reporting period.

A provision is recognised for those matters for which the tax determination is uncertain but it is considered probable that there will 
be a future outflow of funds to a tax authority. The provisions are measured at the best estimate of the amount expected to become 
payable. The assessment is the result of the Group’s judgement based on the advice of external tax professionals and supported by 
previous experience in respect of such activities.

Deferred tax

Deferred tax is the tax expected to be payable or recoverable on differences between the carrying amounts of assets and liabilities 
in the financial statements and the corresponding tax bases used in the computation of taxable profit, and is accounted for using 
the liability method. Deferred tax liabilities are generally recognised for all taxable temporary differences and deferred tax assets are 
recognised to the extent that it is probable that taxable profits will be available against which deductible temporary differences can 
be utilised. Such assets and liabilities are not recognised if the temporary difference arises from the initial recognition of goodwill or 
from the initial recognition (other than in a business combination) of other assets and liabilities in a transaction that affects neither the 
taxable profit nor the accounting profit. 

Deferred tax liabilities are recognised for taxable temporary differences arising on investments in subsidiaries and associates, and 
interests in joint ventures, except where the Group is able to control the reversal of the temporary difference and it is probable that 
the temporary difference will not reverse in the foreseeable future. Deferred tax assets arising from deductible temporary differences 
associated with such investments and interests are only recognised to the extent that it is probable that there will be sufficient taxable 
profits against which to utilise the benefits of the temporary differences and they are expected to reverse in the foreseeable future.

The carrying amount of deferred tax assets is reviewed at each reporting date and reduced to the extent that it is no longer probable 
that sufficient taxable profits will be available to allow all or part of the asset to be recovered.

Deferred tax is calculated at the tax rates that are expected to apply in the period when the liability is settled, or the asset is realised 
based on tax laws and rates that have been enacted or substantively enacted at the reporting date. Deferred tax is charged or 
credited in the income statement, except when it relates to items charged or credited in other comprehensive income, in which case 
the deferred tax is also dealt with in other comprehensive income.

The measurement of deferred tax liabilities and assets reflects the tax consequences that would follow from the manner in which the 
Group expects, at the end of the reporting period, to recover or settle the carrying amount of its assets and liabilities.

Deferred tax assets and liabilities are offset when there is a legally enforceable right to set off current tax assets against current tax 
liabilities and when they relate to income taxes levied by the same taxation authority and the Group intends to settle its current tax 
assets and liabilities on a net basis.

Current tax and deferred tax for the year

Current and deferred tax are recognised in the profit or loss, except when they relate to items that are recognised in other 
comprehensive income or directly in equity, in which case, the current and deferred tax are also recognised in other comprehensive 
income or directly in equity respectively. Where current tax or deferred tax arises from the initial accounting for a business 
combination, the tax effect is included in the accounting for the business combination.

Research and Development Tax Credits
Novacyt UK Holdings Limited subsidiary companies and Primerdesign benefit from tax credits for their research activities. The 
tax credit is calculated per calendar year and deducted from the tax payable by the company in respect of the year during which 
research expenses were incurred. Tax credits that cannot be deducted from tax expense are refunded to the Company are treated as 
subsidies in the income statement. 

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Profit/loss per share
The Group reports basic and diluted profit/loss per common share. Basic profit/loss per share is calculated by dividing the profit 
attributable to common Shareholders of the Company by the weighted average number of common shares outstanding during the 
period.

Diluted profit/loss per share is determined by adjusting the profit attributable to common Shareholders by the weighted average 
number of common shares outstanding, taking into account the effects of all potential dilutive common shares, including options. 
These options are taken into account for the calculation of the profit/loss per share only if their exercise price is higher than the 
market price and if they have a dilutive effect on the result per share. 

Exceptional items
Exceptional items are those costs or incomes that in the view of the Board of Directors, require separate disclosure by virtue of their 
size or incidence, and are charged/credited in arriving at operating profit on the face of the consolidated income statement.

4. CRITICAL ACCOUNTING JUDGEMENTS AND KEY SOURCES OF ESTIMATE 
UNCERTAINTY
In the application of the Group’s accounting policies, which are described in note 3, the Directors are required to make judgements 
(other than those involving estimations) that have a significant impact on the amounts recognised and to make estimates and 
assumptions about the carrying amounts of assets and liabilities that are not readily apparent from other sources. The estimates and 
associated assumptions are based on historical experience and other factors that are considered to be relevant. Actual results may 
differ from these estimates.

The estimates and underlying assumptions are reviewed on an ongoing basis. Revisions to accounting estimates are recognised in 
the period in which the estimate is revised if the revision affects only that period, or in the period of the revision and future periods if 
the revision affects both current and future periods.

Critical accounting judgements
Constraint of revenue

Revenue is only constrained if it is highly probable there will not be a significant reversal of revenue in the future. Highly probable 
is not defined in IFRS 15 and so it is a significant judgement to be exercised by management. The value of revenue related to 
performance obligations fulfilled in the period to which constraint has not been applied is £129,124,000.

Measurement and useful lives of intangible assets

Other intangible assets (except for goodwill) are considered to have a finite economic useful life. They are amortised over their 
estimated useful lives that are reviewed at each reporting date. In the event of impairment, an estimate of the asset’s recoverable 
amount is made.

The main intangible assets requiring estimates and assumptions are the trademarks and the customer relationships identified as a 
result of the acquisition of Primerdesign, Omega Infectious Diseases business and IT-IS International.

The value of the intangible assets is tested whenever there are indications of impairment and reviewed at each annual closing date or 
more frequently should this be justified by internal or external events.

Trademarks

The value of these assets was determined by discounting the cash flows that could be generated by licensing the trademark, 
estimated as a percentage of revenue derived from information available on comparable assets.

This asset is amortised on a straight-line basis over a period of nine years, estimated as its useful life. It is also tested for impairment 
at least annually. Its recoverable amount is determined using forecasts of future cash flows. The total amount of anticipated cash 
flows reflects management’s best estimate of the future benefits and liabilities expected from the operation of the trademark. The 
resulting estimates are subject to discount rate, percentage of revenue and useful life assumptions.

4. CRITICAL ACCOUNTING JUDGEMENTS AND KEY SOURCES OF ESTIMATE 
UNCERTAINTY continued

The carrying amount of the trademarks at 31 December 2020 is £1,114,000 (2019: £522,000; 2018: £631,000) including the new 
trademarks acquired from IT-IS International in 2020 for £843,000. The amortisation charge for the period is £94,000 (2019: £89,000) 
and the cumulative amortisation is £372,000 (2019: £263,000; 2018: £185,000).

Customer relationships

The value of these assets was determined by discounting the additional margin generated by customers after remuneration of the 
contributing assets.

Customer relationships are amortised on a straight-line basis over a period of nine years, estimated as its useful life. It is also tested 
for impairment at least annually. Its recoverable amount is determined using forecasts of future cash flows over an estimated period 
of time. The total amount of anticipated cash flows reflects management’s best estimate of the future benefits and liabilities expected 
from customer relationships. The resulting estimates are subject to assumptions in respect of the discount rate, additional margin 
generated by customers after remuneration of contributing assets and useful lives.

The carrying amount of the customer relationships at 31 December 2020 is £2,950,000 (2019: £2,843,000; 2018: £3,447,000) 
including the new customer relationships from IT-IS International in 2020 for £1,366,000. The amortisation charge for the period is 
£513,000 (2019: £489,000) and the cumulative amortisation is £2,055,000 (2019: £1,460,000; 2018: £1,032,000).

Deferred taxes

Deferred tax assets are only recognised insofar as it is probable that the Group will have future taxable profits against which the 
corresponding temporary difference can be offset. Deferred tax assets are reviewed at each reporting date and derecognised if it is 
no longer probable there will be taxable profits against which the deductible temporary differences can be utilised.

For deferred tax assets on tax loss carry forwards, the Group uses a multi-criteria approach that takes into account the recovery 
timeframe based on the strategic plan, but which also factors in the strategy for the long-term recovery of tax losses in each country. 
On the basis of the analysis performed, considering that the deferred tax losses could not be used within a reasonable period of time, 
the Group has decided not to recognise any deferred tax asset, in relation to carry forward losses.

The Group has, however, recognised a deferred tax asset on the LTIP charge that can be deducted from a tax perspective only when 
the related payments are made. The LTIP charge has been recognised in full during the period. The corresponding tax deduction is 
partly recorded as a reduction of the tax liability for the year and as a deferred tax asset. 

Deferred tax liabilities on temporary differences relate primarily to the assets acquired as part of the IT-IS International acquisition in 
October 2020.

Trade and other receivables

An estimate of the risks of non-receipt based on commercial information, current economic trends and the solvency of individual 
customers is made to determine the need for impairment on a customer-by-customer basis. Management use significant judgement 
in determining whether a credit loss provision is required.

At the year end, the Group had trade receivables of £79,341,000 against which a credit loss of £160,000 has been applied. At the 
date of signing the financial statements, £23,957,000 of the year end receivables were overdue due to a contract dispute (see note 
50). Management expects to be able to recover these balances in full; this is a significant judgement.

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UNCERTAINTY continued
Provisions

The carrying value of provisions as at 31 December 2020, 2019 and 2018 are as per the table below:

Amounts in £‘000
Provisions for restoration of premises
Long-term management incentive plan
Provisions for litigation
Provisions for product warranty
Total provisions

Provisions for restoration of premises

 Year ended 
31 December 
2020 
 242 
 – 
 68 
 19,788 
 20,098 

 Year ended 
31 December 
2019 
 192 
 13 
 43 
–
 248 

 Year ended 
31 December 
2018 
 133 
 18 
 90 
–
 241 

The value of provision required is determined by management on the basis of available information, experience and, in some cases, 
expert estimates. When these obligations are settled, the amount of the costs or penalties that are ultimately incurred or paid may 
differ significantly from the amounts initially provisioned. Therefore, these provisions are regularly reviewed and may have an effect on 
the Group’s future results.

To the Group’s knowledge, there is no indication to date that the parameters adopted as a whole are not appropriate, and there are 
no known developments that could significantly affect the amount of provision.

Provisions for product warranty

The value of provision required is determined by management based on available information, experience and, in some cases, expert 
estimates. Product warranty provisions are only included if it is considered to be probable that an outflow of economic benefit will be 
required. Determination of probable is a significant judgement especially in light of the resolution of the dispute described in note 50.

Key sources of estimation uncertainty
The Group has a number of key sources of estimation uncertainty as listed below. Of these items, only the measurement of goodwill 
(see note 15) is considered likely to give material adjustment. Where there are other areas of estimates these have been deemed not 
material.

Measurement of goodwill

Goodwill is tested for impairment on an annual basis. The recoverable amount of goodwill is determined mainly on the basis of 
forecasts of future cash flows. The total amount of anticipated cash flows reflects management’s best estimate of the future benefits 
and liabilities expected for the relevant CGU. The assumptions used and the resulting estimates sometimes cover very long periods, 
taking into account the technological, commercial and contractual constraints associated with each CGU. These estimates are 
mainly subject to assumptions in terms of volumes, selling prices and related production costs, and the exchange rates of the 
currencies in which sales and purchases are denominated. They are also subject to the discount rate used for each CGU.

The value of the goodwill is tested whenever there are indications of impairment and reviewed at each annual closing date or more 
frequently should this be justified by internal or external events.

4. CRITICAL ACCOUNTING JUDGEMENTS AND KEY SOURCES OF ESTIMATE 
UNCERTAINTY continued
The carrying amount of goodwill on the statement of financial position and related impairment loss over the periods are shown below:

Amounts in £‘000
Goodwill Lab21 Products
Cumulative impairment of goodwill
Net value
Goodwill Primerdesign
Cumulative impairment of goodwill
Net value
Goodwill Omega Infectious Diseases
Derecognition of goodwill
Cumulative impairment of goodwill
Net value
Goodwill IT-IS International 
Cumulative impairment of goodwill
Net value
Total goodwill

 Year ended 
31 December 
2020 
16,022
(14,105)
1,917
6,523
–
6,523
85
 – 
(85)
–
9,437
–
9,437
17,877

 Year ended 
31 December 
2019 
 15,122 
(7,772)
 7,350 
 6,157 
 – 
 6,157 
 285 
(200) 
– 
 85 
 – 
 – 
 – 
 13,592 

 Year ended 
31 December 
2018 
 15,968 
(8,206)
 7,762 
 6,501 
 – 
 6,501 
 285 
– 
 – 
 285 
 – 
 – 
 – 
 14,548 

Sensitivity analysis has been performed on the goodwill balance and there is significant headroom associated with the Primerdesign 
balance, but there is limited headroom on the Lab21 Products goodwill, which could result in future impairments.

Litigations

The Group may be party to regulatory, judicial or arbitration proceedings that, in view of the relating uncertainties, may have an 
impact on the Group’s financial position.

The Group’s management regularly reviews current proceedings, their progress and assesses the need to establish appropriate 
provisions or to change their amount if the occurrence of events during the course of the proceedings necessitates a reassessment 
of the risk. Internal or external advisors are involved in determining the costs that may be incurred.

The decision to set aside provisions to cover a risk and the amount of such provisions are based on the risk assessment on a case-
by-case basis, management’s assessment of the unfavourable nature of the outcome of the proceeding in question (probability) and 
the ability to reliably estimate the associated amount.

5. REVENUE
The table below shows revenue from ordinary operations:

Amounts in £‘000
Manufactured goods
Services
Traded goods
Other
Total revenue

Year ended 
31 December 
2020
276,874
290
40
–
277,204

Year ended 
31 December 
2019  
10,792
311
39
326
11,468

A portion of the Group’s revenue is generated in foreign currencies (particularly in Euros and US Dollars). The Group has not hedged 
against the associated currency risk.

The breakdown of revenue by operating segment and geographic area is presented in note 6.

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Segment reporting
Pursuant to IFRS 8, an operating segment is a component of an entity:

•  that engages in business activities from which it may earn revenues and incur expenses (including revenues and expenses relating 

to transactions with other components of the same entity);

•  whose operating results are regularly reviewed by the Group’s Chief Executive and the managers of the various entities to make 

decisions regarding the allocation of resources to the segment and to assess its performance; and

•  for which discrete financial information is available.

The Group has identified four operating segments, whose performances and resources are monitored separately:

Primerdesign (formerly Molecular Products)

This segment represents the activities of Primerdesign, which is a designer, manufacturer and marketer of molecular ‘real-time’ qPCR 
testing devices and reagents in the areas of infectious diseases based in Southampton, UK. 

Lab21 Products (formerly Corporate and Diagnostics)

This segment represents the activities of Lab21 Products, which is a developer, manufacturer and distributor of a large range of 
protein-based infectious disease IVD products with both Microgen Bioproducts Ltd and Lab21 Healthcare Ltd, now based in 
Camberley, UK.

IT-IS International 

This segment represents the activities of IT-IS International, a UK based diagnostic instrument development and manufacturing 
company specialising in the development of PCR devices for the life sciences and food testing industry.

Corporate

This segment represents Group central/corporate costs and the results of Novacyt UK Holdings Limited. Where appropriate, central 
corporate costs are recharged to individual business units via a management recharge process.

Intercompany Eliminations 

This column represents intercompany transactions across the Group that have not been allocated to an individual operating segment, 
but is not a discreet segment.

The Chief Operating Decision Maker is the Chief Executive Officer. 

Headcount
The average headcount by segment is presented in the table below:

Segment
Primerdesign
Lab21 Products
IT-IS International
Corporate
Discontinued operations
Total headcount

2020
81
47
36
10
–
174

2019
48
60
–
6
11
125

6. OPERATING SEGMENTS continued
Reliance on major customers and concentration risk
Primerdesign’s revenue includes approximately £190,000,000 (2019: £nil) from sales to the Group’s largest customer. No other 
customers contributed 10% or more to the Group’s revenue in 2020.

91% of loans and receivables are with one counterparty, with whom there is a contract dispute as disclosed in note 50. Management 
considers it to be more likely than not that the year end balances are recoverable. £47,926,000 of the year end receivables balance 
of £71,883,000 with the counterparty in question has been received in 2021.

Breakdown of revenue by operating segment and geographic area
At 31 December 2020

Primerdesign 

Lab21 
Products 

IT-IS 
International

 Total 

Amounts in £‘000
Geographical area 
United Kingdom
Europe (excluding UK)
Africa 
Asia-Pacific 
America
Middle East 
Total revenue 

At 31 December 2019

Amounts in £‘000
Geographical area 
United Kingdom
Europe (excluding UK)
Africa 
Asia-Pacific 
America
Middle East 
Total revenue 

Breakdown of result by operating segment
Year ended 31 December 2020

218,552
30,917
2,896
5,305
9,655
5,492
272,817

591
1,058
151
920
340
250
3,310

246
56
6
453
316
–
1,077

Primerdesign 

 Lab21 
Products 

1,097
 1,249
 312
 712
 1,696
 463
 5,529 

986
 1,476
 560
 1,529
 647
 741
 5,939 

219,389
32,031
3,053
6,678
10,311
5,742
277,204

 Total 

2,083
2,725
 872
 2,241
2,343
1,204
11,468 

Total
277,204
(65,704)
(4,492)
(1,630)
(29,230)
(3)

Amounts in £‘000
Revenue
Cost of sales
Sales and marketing costs
Research and development
General and administrative
Governmental subsidies
Earnings before interest, tax,  
depreciation and amortisation  
as per management reporting
Depreciation and amortisation
Operating profit/(loss)  
before exceptional items

Primerdesign
272,817
(63,987)
(3,550)
(1,515)
(25,133)
–

Lab21 
Products
5,203
(3,088)
(929)
(3)
(2,138)
(3)

IT-IS 
International
6,905
(1,627)
9
(112)
(245)
–

Corporate
–
–
(22)
–
(1,725)
–

Intercompany 
Eliminations
(7,721)
2,998
–
–
11
–

178,632
(795)

(958)
(416)

4,930
(70)

(1,747)
(21)

(4,712)
–

176,145
(1,302)

177,837

(1,374)

4,860

(1,768)

(4,712)

174,843

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Year ended 31 December 2019

Amounts in £‘000
Revenue
Cost of sales
Sales and marketing costs
Research and development
General and administrative
Governmental subsidies
Earnings before interest, tax, depreciation and 
amortisation as per management reporting
Depreciation and amortisation
Operating profit/(loss) before exceptional items

Primerdesign
5,531
(808)
(1,266)
(362)
(1,715)
–

1,380
(734)
646

Lab21 
Products
6,037
(3,418)
(1,096)
(33)
(1,685)
3

(192)
(519)
(711)

Corporate
–
–
(6)
–
(1,007)
–

(1,013)
(9)
(1,022)

Intercompany 
Eliminations
(100)
98
1
–
–
–

(1)
–
(1)

Total
11,468
(4,128)
(2,367)
(395)
(4,407)
3

174
(1,262)
(1,088)

Segment assets and liabilities are not reported to the Chief Operating Decision Maker on a segmental basis and are therefore not 
disclosed.

7. COST OF SALES

Amounts in £‘000
Cost of inventories recognised as an expense
Change in stock provision
Non-stock items and supplies
Freight costs
Direct labour
Product warranty
Other
Total cost of sales

Year ended 
31 December 
2020
20,113
2,978
2,088
284
20,243
19,753
245
65,704

Year ended 
31 December 
2019
2,693
–
32
73
1,288
–
42
4,128

The cost of inventories recognised as an expense has increased significantly due to the higher sales volumes in 2020. Some 
elements of manufacturing were outsourced to meet market demands in 2020; these costs are included in direct labour. A 2020 
stock provision has been made for inventory that is deemed as being at risk of not being sold.

A product warranty cost has been estimated for the year; this is significantly higher due to the higher sales volumes in 2020  
(see note 30) and the notification of a product warranty claim after the year end (see note 50).

8. SALES, MARKETING AND DISTRIBUTION EXPENSES

Amounts in £‘000
Advertising expenses
Distribution expenses
Employee compensation and social security contributions
Travel and entertainment expenses
Other sales and marketing expenses
Total sales, marketing and distribution expenses 

Year ended 
31 December 
2020
314 
495 
3,238 
103 
342 
4,492 

Year ended 
31 December 
2019
160 
334 
1,580 
222 
71 
2,367 

A significant number of new sales and marketing employees were hired during 2020 to support and deliver the 2020 revenue growth. 

9. RESEARCH AND DEVELOPMENT EXPENSES

Amounts in £‘000
Employee compensation and social security contributions
Other expenses 
Total research and development expenses

Year ended 
31 December 
2020
939
691
1,630

Year ended 
31 December 
2019
329
66
395

A significant number of new research and development employees were hired during 2020 to support and deliver the 2020 revenue 
growth seen in the business. Other expenses predominantly include consumables, non-capitalised development costs and quality 
control/assurance expenses.

10. GENERAL AND ADMINISTRATIVE EXPENSES

Amounts in £‘000
Purchases of non-stored raw materials and supplies
Lease and similar payments
Maintenance and repairs
Insurance premiums
Legal and professional fees
Banking services
Employee compensation and social security contributions
Depreciation and amortisation of property, plant and equipment, and intangible assets
Other general and administrative expenses
Total general and administrative expenses

Year ended 
31 December 
2020
373 
337 
278 
574 
2,350 
231 
23,904 
1,302 
1,183
30,532 

Year ended 
31 December 
2019
296 
159 
106 
100 
757 
70 
2,459 
1,267 
455
5,669

Novacyt granted phantom awards to certain employees under a long-term management incentive plan adopted on 1 November 
2017. The exercise price was set at the closing share price on the grant date. The phantom awards will be settled in cash in three 
tranches. The phantom awards vested on the third anniversary of the grant date, 1 November 2020, resulting in significantly higher 
employee compensation costs in 2020. 

Legal and professional fees include advisors’ fees, auditor fees and legal fees; all of which have increased as the business has grown  
in 2020.

Other general and administrative expenses include recruitment fees, building rates charges and regulatory fees.

100

101

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNotes to the annual accounts continuedfor the years ended 31 December 2020 and 31 December 201911. OTHER OPERATING INCOME AND EXPENSES

Amounts in £‘000
Litigations with employees
Other operating income
Total other operating income
Impairment of Lab21 Products goodwill
Impairment of Omega Infectious Diseases business intangible assets 
Restructuring expenses
Result of the sale of Lab21 Ltd
Business sale expenses
Acquisition related expenses
Other expenses

Total other operating expenses

Operating income

Year ended 
31 December 
2020
– 
– 
– 
(5,768) 
(1,111) 
(106) 
– 
(79) 
(187) 
(151) 
(7,402) 

Year ended 
31 December 
2019
39 
72 
111 
–
–
(166) 
(46) 
(253) 
– 
(114) 
(579) 

Other operating income predominantly relates to the settlement of a legal claim against a third party.

Operating expenses

Goodwill associated with Lab21 Products has been impaired following changes in market conditions, which have reduced future 
expected cashflow generation.

The remaining intangible assets associated with the Omega Infectious Diseases business have been fully impaired.

Restructuring expenses include costs associated with the closure of the Axminster and Bridport sites, along with other Company-
wide restructuring fees, including redundancy payments.

Business sale expenses in 2019 relate to the disposal of the NOVAprep business in France and the sale of Lab21 Ltd in the UK.

Acquisition related expenses relate to the October 2020 purchase of IT-IS International Ltd.

12. FINANCIAL INCOME AND EXPENSE

Amounts in £‘000
Financial foreign exchange gains
Discount of financial instruments
Change in fair value of options
Other financial income
Total financial income
Interest on loans 
Financial foreign exchange losses
Change in fair value of options
Discount of financial instruments
Other financial expense
Total financial expense

102

Year ended  
31 December 
2020
32 
46
– 
5
83

(1,601) 
(353) 
– 
(12) 
(387) 
(2,353) 

Year ended 
31 December 
2019
200 
–
27 
1 
228
(958) 
(114)
(684)
(81)
(261)
(2,098) 

12. FINANCIAL INCOME AND EXPENSE continued
Interest on loans

The 2020 interest charge mainly relates to the full settlement of the Harbert European Growth Capital bond notes that amounted to 
£1,379,000. It also includes £185,000 interest charges in connection with IFRS 16 “Lease Liabilities”.

In 2019, the interest charge mainly related to the Kreos, Vatel, Negma Group Ltd (“Negma”), and Harbert European Growth Capital 
bond notes.

Financial foreign exchange losses

Financial foreign exchanges losses in 2020 are driven by exchange movements on the €5,000,000 Harbert European Growth Capital 
bond that was repaid in the year and revaluations of bank and intercompany accounts held in foreign currencies.

Change in fair value of options 

The December 2019 balance relates to the revaluation of Harbert European Growth Capital warrants liability of £684,000.

Other financial expenses

In November 2019, Novacyt SA granted Negma 1,300,000 phantom warrants, i.e. warrants that do not give access to the share 
capital of the Company, in exchange for the cancellation of 1,300,000 warrants giving access to the share capital of Novacyt SA. The 
phantom warrants guaranteed to pay Negma the profit from the difference between the €0.20 exercise price and the share price on 
the day before the exercise date. This instrument was recognised as a derivative financial liability at December 2019 for a value of 
£77,000. Negma exercised the phantom warrants in February 2020, which resulted in a payment to Negma of £439,000. The charge 
at December 2020 is the difference between these two amounts.

The costs in 2019 relate to additional interest and settlement fees to fully remove and pay down the monies owed to Negma, Kreos 
and the original Primerdesign owners.

13. INCOME TAX
The Group’s tax charge is the sum of the total current and deferred tax expense.

Amounts in £‘000
Current tax expense
Current year (charge)/income
Deferred tax expense
Deferred tax

Total income tax (expense)/income in the income statement 

The charge for the year can be reconciled to the profit in the income statement as follows:

Amounts in £‘000
Profit/(loss) before taxation
Tax at the French corporation tax rate (2020 and 2019: 28%)
Effect of different tax rate of subsidiaries in other jurisdictions
Effect of non-deductible expenses
Losses not recognised for deferred tax
Research tax expenditure enhancement
Other adjustments
Total tax (expense)/income for the year

Year ended 
31 December 
2020

Year ended 
31 December 
2019

(35,605)

2,857 

(32,748) 

7 

– 

7

Year ended 
31 December 
2020
165,171
(46,248)
15,593
(1,696)
(669)
169
103
(32,748)

Year ended 
31 December 
2019

(5,756) 
1,612
331
(575)
(1,374)
96
(83)
7

103

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNotes to the annual accounts continuedfor the years ended 31 December 2020 and 31 December 2019 
13. INCOME TAX continued
As at 31 December 2020, the Group has unused tax losses of £41,230,000 (2019: £37,445,000) available for offset against future 
relevant profits. Their period of use is unlimited.

The key item making up the non-deductible expenses in 2020 is the impairment of the goodwill attached to the Lab21 Products. In 
2019, the non-deductible expenses relate to the change in fair value of the warrants recorded in Novacyt and the amortisation of the 
intangible assets acquired with Primerdesign.

Matters affecting the tax charge
During 2020, Novacyt applied for a number of patents for technology it developed during the period. Patents can take several years 
to be granted, if at all, and at the year end, all the patents were still going through the process for approval. If one or more of the 
patents ultimately are granted then the Group hopes to be able to benefit from the UK Patent Box regime, which is a special low 
corporate tax rate used by several countries to incentivise research and development by taxing revenues from patented products 
differently from other revenues. Subject to a number of adjustments, the effective rate of tax on profits derived from the sale of 
products subject to patents is close to 10% rather than the current UK corporation tax rate of 19% (due to rise to 25% in 2023). The 
Patent Box rate can only be claimed once a patent has been granted, although the benefit can be backdated to the time at which 
the patent was applied for, and so this is not reflected in the 2020 accounts.

14. PROFIT/LOSS PER SHARE
The profit or loss per share is calculated based on the weighted average number of shares outstanding during the period. The 
diluted profit or loss per share is calculated based on the weighted average number of shares outstanding and the number of shares 
issuable as a result of the conversion of dilutive financial instruments.

Amounts in £’000
Net profit/(loss) attributable to owners of the Company
Impact of dilutive instruments
Net diluted profit/(loss) attributable to owners of the Company
Weighted average number of shares
Impact of dilutive instruments
Weighted average number of diluted shares
Profit/(loss) per share (in £)
Diluted profit/(loss) per share (in £)

Year ended 
31 December 
2020
 132,423 
 – 
 132,423 
 68,187,101 
 – 
 68,187,101 
 1.94 
 1.94 

Year ended 
31 December 
2019
(5,749)
–
(5,749)
 45,731,091 
 – 
 45,731,091 
(0.13)
(0.13)

Pursuant to IAS 33, options whose exercise price is higher than the value of the Company’s security were not taken into account in 
determining the effect of dilutive instruments.

The calculation of earnings per share does not take into account potential anti-dilutive actions, which would have the effect of 
increasing earnings per share.

104

14. PROFIT / LOSS PER SHARE continued
The table below presents the movements of the stock options during 2020. They were not taken into account in the calculation of 
diluted earnings because they were anti-dilutive for the period ending 31 December 2019, and were all exercised or elapsed at 31 
December 2020.

Beneficiary

Kreos

Primerdesign

Grant date
Number of warrants

Exercise price

Exercise deadline

Accounting
Number of warrants on  
1 January 2020
Warrants exercised in 2020
Number of additional shares
Share capital increase
Warrants cancelled in 2020
Warrants outstanding on  
31 December 2020

12 May 2016
353,536

12 May 2016
1,000,000

€1.45
1 November 
2022

Equity

353,536
(353,536)
353,536
€512,627
–

€1.16

12 May 2021
Derivative 
financial liability

1,000,000
(1,000,000)
1,000,000
€1,160,000
–

Yorkville
31 July 2015 
to  
18 July 2017
1,501,427
From €5.511 
to €0.946
3 years after 
issuance

Equity

853,216
(528,541)
528,541
€500,000
(324,675)

Negma

Harbert

Total

25 April 2019
2,979,544

€0.20

25 April 2024
Derivative 
financial liability

5 November 
2019
6,017,192

€0.0698
5 November 
2026
Derivative 
financial liability

1,679,544
(1,679,544)
1,679,544
€335,909
–

6,017,192
(6,017,192)
6,017,192
€420,000
–

9,903,488
(9,578,813)
9,578,813
€2,928,536
(324,675)

–

–

–

–

–

–

15. GOODWILL
Goodwill is the difference recognised, upon consolidation of a company, between the fair value of the purchase price of its shares 
and the net assets acquired and liabilities assumed, measured in accordance with IFRS 3.

Cost
At 1 January 2019
Derecognition on acquisition of the Omega Infectious Diseases business
Exchange differences
At 31 December 2019
Write-off of the Omega Infectious Diseases goodwill
Recognition of goodwill on acquisition of IT-IS International Ltd
Exchange differences
At 31 December 2020

Accumulated impairment losses
At 1 January 2019
Exchange differences
At 31 December 2019
Impairment of the Lab21 Products goodwill
Exchange differences
At 31 December 2020
Carrying value at 31 December 2018
Carrying value at 31 December 2019
Carrying value at 31 December 2020

£’000
22,754
(200)
(1,190)
21,364
(85)
9,437
1,266
31,982

8,206
(434)
7,772
5,767
566
14,105
14,548
13,592
17,877

105

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Sensitivity of the value derived from the discounted cash flow model to changes to the 
assumptions used for the Primerdesign acquisition

Terminal growth rates

180,961 
15.0%
16.0%
17.0%
18.0%
19.0%
19.8%
20.0%
21.0%
22.0%

0.0%
183,663 
182,871 
182,172 
181,552 
180,997 
180,595 
180,499 
180,049 
179,641 

0.5%
183,906 
183,076 
182,347 
181,702 
181,127 
180,711 
180,612 
180,148 
179,727 

1.0%
184,165 
183,294 
182,532 
181,860 
181,264 
180,833 
180,730 
180,251 
179,818 

1.5%
184,444 
183,528 
182,730 
182,029 
181,408 
180,961 
180,855 
180,360 
179,913 

2.0%
184,745 
183,778 
182,941 
182,208 
181,562 
181,097 
180,987 
180,474 
180,013 

2.5%
185,069 
184,047 
183,166 
182,398 
181,724 
181,241 
181,127 
180,595 
180,118 

3.0%
185,421 
184,337 
183,407 
182,601 
181,896 
181,393 
181,275 
180,722 
180,228 

s
e
t
a
r

C
C
A
W

This sensitivity table shows the difference in the recoverable amounts of the Enterprise Value depending on change in the discount 
rate (WACC) and the perpetual growth rate. The sensitivity analysis shows that an increase of 1% in the WACC would not result in the 
need to impair the Primerdesign goodwill.

IT-IS International
On 15 October 2020, Novacyt UK Holdings Ltd completed the purchase of the entire share capital of IT-IS International Ltd, a 
company incorporated in England and Wales. The company specialises in the development and manufacturing of PCR diagnostic 
instruments for the life sciences and food testing industry.

The calculation of the goodwill is presented in the note 40 “Business combinations”.

IFRS 3 provides for a period of 12 months from the acquisition to complete the identification and measurement of the fair value of 
assets acquired and liabilities assumed. Until October 2021, the gross amount of goodwill is subject to adjustment.

15. GOODWILL continued
Lab21 Products
The impairment testing of the CGU as of 31 December 2020 was conducted by the discounted cash flow (“DCF”) method, with the 
key assumptions as follows:

•  Five-year business plan.

•  Extrapolation of cash flows beyond five years based on a growth rate of 1.5%; and

•  Discount rate corresponding to the expected rate of return on the market for a similar investment, regardless of funding sources, 

equal to 15%.

The implementation of this approach demonstrated that the value of the Enterprise Value amounted to £1,917,000, which is lower 
than the carrying amount of this asset. As such, an impairment charge was recognised in the year ended 31 December 2020.

Sensitivity of the value derived from the Discounted Cash Flow model to changes to the 
assumptions used for the Lab21 acquisition

s
e
t
a
r

C
C
A
W

1,917 
12.5%
13.0%
13.5%
14.0%
14.5%
15.0%
15.5%
16.0%
16.5%

0.0%
2,315 
2,190 
2,075 
1,968 
1,869 
1,777 
1,692 
1,612 
1,537 

0.5%
2,387 
2,255 
2,133 
2,021 
1,917 
1,821 
1,731 
1,648 
1,570 

Terminal growth rates

1.0%
2,464 
2,324 
2,196 
2,078 
1,968 
1,867 
1,774 
1,687 
1,605 

1.5%
2,549 
2,400 
2,263 
2,139 
2,023 
1,917 
1,819 
1,728 
1,643 

2.0%
2,641 
2,482 
2,337 
2,204 
2,083 
1,971 
1,868 
1,772 
1,683 

2.5%
2,742 
2,572 
2,417 
2,276 
2,147 
2,029 
1,920 
1,819 
1,726 

3.0%
2,854 
2,670 
2,504 
2,354 
2,217 
2,091 
1,976 
1,870 
1,772 

This sensitivity table shows the difference in the recoverable amounts of the Enterprise Value depending on change in the discount 
rate (WACC) and the perpetual growth rate. The sensitivity analysis shows that an increase of 1% in the WACC would result in the 
need to impair the Lab21 goodwill further.

The Lab21 Products goodwill relates to Microgen Bioproducts and Lab21 Healthcare.

Omega Infectious Diseases
The decrease in the Omega Infectious Diseases goodwill in 2019 results from the adjustment of the acquisition price of the business. 
Contingent consideration amounting to £200,000 will not be paid, as the contractual conditions will not be achieved. The remaining 
goodwill totalling £85,000 has been fully impaired in the year ended 31 December 2020.

Primerdesign
The impairment testing of the CGU as of 31 December 2020 was conducted by the DCF (discounted cash flow) method, with the 
key assumptions as follows:

•  Five-year business plan;

•  Extrapolation of cash flows beyond five years based on a growth rate of 1.5%; and

•  Discount rate corresponding to the expected rate of return on the market for a similar investment, regardless of funding sources, 

equal to 19.8%.

The implementation of this approach demonstrated that the value of the Enterprise Value amounted to £180,961,000, which is 
greater than the carrying amount of this asset. As such, no impairment was recognised in the year ended 31 December 2020.

106

107

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16. OTHER INTANGIBLE ASSETS

17. PROPERTY, PLANT AND EQUIPMENT

Customer 
relationships

Trademarks

Development 
costs

Patents

Other

Total

 4,479 
– 
– 
– 
– 
(176)
 4,303 
– 
1,366

(851) 
 – 
 187 
 5,005 

(1,032) 
(489) 
– 
– 
– 
– 
 61 
(1,460) 
(513) 
– 
(82) 
(2,055) 

 816 
– 
– 
– 
– 
(31) 
 785 
– 
843
(175) 
–
 33 
 1,486 

(185) 
(89) 
– 
– 
– 
– 
 11 
(263) 
(94) 
– 
(15) 
(372) 

 3,447 
 2,843 
 2,950 

 631 
 522 
 1,114

 398 
 53 
– 
– 
– 
– 
 451 
 111 
–
(285) 
– 
– 
 277 

(114) 
(76)
– 
– 
– 
– 
– 
(190) 
(67) 
104 
– 
(153) 

 284 
 261 
 124 

 91 
 37 
– 
(1,354) 
 1,288 
– 
 62 
 30 
–
(2) 
(1) 
– 
 89 

(69) 
(106) 
(63) 
– 
 752 
(561) 
– 
(47) 
(7)
– 
– 
(54) 

 22 
 15 
 35 

 244 
 9 
(9)
(78) 
 67 
(3) 
 230 
 27 
–
–
– 
 3 
 260 

(170) 
(36) 
– 
 9 
 73 
(67) 
 3 
(188) 
(37) 
– 
(3) 
(228) 

 74 
 42 
 32 

 6,028 
 99 
(9)
(1,432)
 1,355 
(210) 
 5,831 
 168 
2,209
(1,313) 
(1) 
 223 
 7,117 

(1,570) 
(796) 
(63)
 9 
 825 
(628) 
 75 
(2,148)
(718) 
 104 
(100) 
(2,862) 

 4,458 
 3,683 
 4,255

Amounts in £‘000
Cost
At 1 January 2019
Acquisitions
Disposal of businesses
Other disposals
Reclassifications
Foreign exchange impact
At 31 December 2019
Acquisitions
Acquisition of businesses
Other disposals
Reclassifications
At 31 December 2020

Depreciation
At 1 January 2019
Depreciation for the year
Exceptional impairment
Disposal of businesses
Other disposals
Reclassifications
Foreign exchange impact
At 31 December 2019
Depreciation for the year
Acquisition of businesses
Other disposals
Foreign exchange impact
At 31 December 2020

Net book value
At 1 January 2019
At 31 December 2019
At 31 December 2020

Amounts in £‘000
Cost
At 1 January 2019
Acquisitions
Disposal of businesses
Other disposals
Reclassifications
Foreign exchange impact
At 31 December 2019
Acquisitions
Acquisition of businesses
Other disposals
Reclassifications
Foreign exchange impact
At 31 December 2020

Amortisation
At 1 January 2019
Amortisation for the year
Exceptional impairment
Disposal of businesses
Other disposals
Reclassifications
Foreign exchange impact
At 31 December 2019
Amortisation for the year
Other disposals
Foreign exchange impact
At 31 December 2020

Net book value
At 1 January 2019
At 31 December 2019
At 31 December 2020

108

Leasehold 
improvements

Plant and 
machinery

Fixtures and 
fittings

 919 
 23 
(29) 
(50) 
 58 
 1 
 922 
 34 
– 
– 
(79) 
 877 

(217) 
(125) 
– 
 30 
 36 
(58) 
 2 
(332) 
(89) 
– 
– 
– 
(421) 

 702 
 590 
 456 

 1,000 
 151 
(53) 
(1,289) 
 1,201 
 1 
 1,011 
 686 
 46 
(6) 
 56 
 1,793 

(695) 
(271) 
(129)
 54 
 1,319 
(1,090) 
 3 
(809)
(139) 
(29) 
 6 
– 
(971) 

 305 
 202 
 822 

 333 
 22 
(46) 
(121) 
 78 
 1 
 267 
 253 
 143 
(16) 
 115 
 762 

(266) 
(48) 
– 
 45 
 127 
(69) 
(2) 
(213) 
(67) 
(131) 
 14 
(1) 
(397) 

 67 
 54 
 365

Total

 2,252 
 196 
(128) 
(1,460) 
 1,337 
 3 
 2,200 
 973 
 189 
(22)
 92 
 3,432 

(1,178) 
(444) 
(129) 
 129 
 1,482 
(1,217) 
 3 
(1,354) 
(295) 
(160) 
 20 
(1) 
(1,789) 

 1,074 
 846 
 1,643 

109

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18. RIGHT-OF-USE ASSETS

Amounts in £‘000
Cost
At 1 January 2019
Adoption of IFRS 16
Reclassifications
At 31 December 2019
Additions
Acquisition of businesses
Reclassifications
At 31 December 2020

Depreciation
At 1 January 2019
Depreciation for the year
At 31 December 2019
Depreciation for the year
Acquisition of businesses
Reclassifications
At 31 December 2020

Net book value
At 1 January 2019
At 31 December 2019
At 31 December 2020

19. NON-CURRENT FINANCIAL ASSETS

Amounts in £‘000
Rental deposits
Guarantee deposit 
Other
Total non-current financial assets

Land and 
buildings

Plant and 
machinery

– 
 2,252 
– 
 2,252 
 396 
 97 
– 
 2,745 

–
(233) 
(233) 
(256)
(18) 
– 
(507) 

– 
 54 
 82 
 136 
 41 
– 
(123) 
 54 

–
(30) 
(30) 
(32) 
– 
 29 
(33) 

Total

– 
 2,306 
 82 
 2,388 
 437 
 97 
(123) 
 2,799 

–
(263) 
(263) 
(288) 
(18)
 29 
(540) 

– 
 2,019 
 2,238 

– 
 106 
 21 

– 
 2,125 
 2,259 

 Year ended 
31 December 
2020 
 124 
–
 14 
 138 

 Year ended 
31 December 
2019 
 109 
 80 
 6 
 195 

 Year ended 
31 December 
2018 
 115 
 85 
 3 
 203

20. DEFERRED TAX ASSETS AND LIABILITIES
The table below shows the movements in deferred tax assets and liabilities during the reporting period:

Amounts in £‘000
At 1 January 2019
Credit/(charge) to income statement
At 31 December 2019
Credit/(charge) to income statement
Acquisition of IT-IS International
At 31 December 2020

Accelerated 
capital 
allowances
(49)
7
(42)
(194)
(2)
(238)

Intangible 
assets 
–
–
–
10
(499)
(489)

Intra-Group 
profit
–
–
–
897
–
897

Long-term 
incentive plan
–
–
–
2,125
–
2,125

Other 
temporary 
differences
–
–
–
19
(92)
(73)

Total
(49)
7
(42)
2,857
(593)
2,222

At 31 December 2020, deferred tax liabilities amounting to £489,000 result from the recognition of brand and customer relationships 
intangible assets as part of the October 2020 IT-IS International acquisition.

A £2,125,000 deferred tax asset relates to the portion of the Long-Term Incentive Plan charge that has been recognised by Novacyt 
UK Holdings, but will not be deducted for taxation until payments are made in 2021 and 2022. 

A £897,000 deferred tax asset arises from the elimination of the internal margin on intercompany stock held at 31 December 2020.

Deferred tax assets and liabilities are recognised on the statement of financial position as follows:

Amounts in £‘000
Deferred tax assets
Deferred tax liabilities
Net deferred tax assets/(liabilities)

Year ended 
31 December 
2020 
3,022
(800)
2,222

Year ended 
31 December 
2019 
–
(42)
(42)

Year ended 
31 December 
2018 
–
(48)
(48)

Novacyt SA and Lab21 Healthcare Ltd have tax losses carried forward for use against future taxable profits. However, no deferred tax 
assets have been recognised for these losses as there is insufficient evidence that there will be future profits in these companies to 
use the losses against.

The following table shows the deferred tax assets not presented in the statement of financial position:

Amounts in £‘000
Novacyt SA
Lab21 Healthcare Ltd
Microgen Bioproducts Ltd
Novacyt UK Holdings Ltd
Total unrecognised deferred tax assets

Year ended 
31 December 
2020 
10,004
1,045
–
–
11,049

Year ended 
31 December 
2019 
8,725
1,005
135
54
9,919

Year ended 
31 December 
2018 
7,562
823
75
–
8,460

110

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Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNotes to the annual accounts continuedfor the years ended 31 December 2020 and 31 December 201921. OTHER LONG-TERM ASSETS

Amounts in £‘000
Long-term receivable from the sale of the NOVAprep business
Long-term receivable from the sale of Lab21 Limited
Total other long-term assets

 Year ended 
31 December 
2020 
–
96
96

 Year ended 
31 December 
2019 
87
96
183

 Year ended 
31 December 
2018 
–
–
–

Lab21 Limited was sold in July 2019. The purchase consideration was split into milestone payments and the long-term portion of the 
sale price has been discounted to £96,000.

The assets of NOVAprep were sold in December 2019. The purchase consideration was split into milestone payments and the long-
term portion has been discounted to £87,000. Due to uncertainty over the recoverability of the outstanding NOVAprep milestone 
payments, the balance due has been written off in 2020.

22. INVENTORIES AND WORK IN PROGRESS

Amounts in £‘000
Raw materials
Work in progress
Finished goods
Traded goods
Stock provisions
Total inventories and work in progress

 Year ended 
31 December 
2020 
14,406
8,999
9,550
–
(3,067)
29,888

 Year ended 
31 December 
2019 
1,195
241
666
70
(89)
2,083

 Year ended 
31 December 
2018 
941
509
666
–
–
2,116

Increased inventory levels are supporting the Group’s revenue growth, with significant finished goods being held in stock ready for 
immediate dispatch, as demand remains high. 

The lead time for obtaining some raw materials is significant, so bulk orders have been placed to ensure there are no supply chain 
issues; these contribute to the higher raw materials balance in 2020.

The closing inventory balance is assessed every year and a stock provision is made for stock at risk of not being sold.

23. TRADE AND OTHER RECEIVABLES

Amounts in £‘000
Trade and other receivables
Estimated credit loss provision
Accrued income
Tax receivables (excluding income tax)
Receivables on sale of businesses
Other receivables
Total trade and other receivables

 Year ended 
31 December 
2020 
79,341 
(160) 
– 
343 
67 
1 
79,592 

 Year ended 
31 December 
2019 
1,720 
(397) 
15 
335 
152 
26 
1,851 

 Year ended 
31 December 
2018 
3,005 
(42) 
88 
444 
– 
22 
3,517 

23. TRADE AND OTHER RECEIVABLES continued
The movement in the allowance for doubtful debts is shown below:

Amounts in £‘000
Balance at the beginning of the period
Impairment losses recognised
Amounts written off during the year as uncollectible
Amounts recovered during the year
Change in the scope of consolidation
Balance at the end of the period

The split by maturity of the clients’ receivables is presented below:

Amounts in £‘000
Less than one month
Between one and three months
Between three months and one year
More than one year
Balance at the end of the period

24. PREPAYMENTS AND SHORT-TERM DEPOSITS

Amounts in £‘000
Liquidity contract
Prepaid expenses
Total prepayments and short-term deposits

 Year ended 
31 December 
2020 
397
163
(400)
– 
– 
160

 Year ended 
31 December 
2019 
42
382
(5)
(14)
(8)
397

 Year ended 
31 December 
2020 
77,944
1,364
6
27
79,341

 Year ended 
31 December 
2019 
1,029
101
116
473
1,720

Year ended 
31 December 
2018
2,101
201
206
497
3,005

 Year ended 
31 December 
2020 
 103 
 3,628 
 3,731 

 Year ended 
31 December 
2019 
9
 347 
 356 

 Year ended 
31 December 
2018 
8 
 210 
 218 

The key balances at December 2020 include prepayments for the annual group commercial insurance, prepayments for stock that 
was not delivered to Primerdesign in 2020, rent, rates and prepaid support costs.

The balances at December 2019 and December 2018 cover items such as rent, insurances and prepaid support agreements. 

25. CASH AND CASH EQUIVALENTS
The net cash available to the Group includes the following items:

Amounts in £‘000
Money market deposits
Available cash
Total cash and cash equivalents

Year ended 
31 December 
2020
–
91,765
91,765

Year ended 
31 December 
2019
11
1,531
1,542

Year ended 
31 December 
2018
12
1,009
1,021

Trade receivables balances are due within one year. Once an invoice is more than 90 days overdue, it is deemed more likely to default 
and as such, these invoices have been provided for in full as part of an expected credit loss model.

Cash has significantly increased due to the increased profitability of the Group in 2020. 

112

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The following tables show borrowings and financial liabilities carried at amortised cost, excluding lease liabilities (see note 27).

Maturities as of 31 December 2019

Amounts in £‘000
Bond notes
Accrued interest on borrowings
Short-term financing facilities
Total financial liabilities

Maturities as of 31 December 2018

Amounts in £‘000
Bond notes
Accrued interest on borrowings
Short-term financing facilities
Total financial liabilities

Amount due 
for settlement 
within 12 
months
1,116
32
721
1,869

Amount due 
for settlement 
after 12 
months
5,240
–
–
5,240

Amount due 
for settlement 
within 12 
months
2,684
64
61
2,809

Amount due 
for settlement 
after 12 
months
2,019
–
18
2,037

Change in borrowings and financial liabilities in 2020

Amounts in £‘000
Bond notes
Accrued interest on borrowings
Short-term financing facilities
Total financial liabilities

At 31 
December 
2019
6,356
32
721
7,109

Repayment
(4,592)
(32)
(721)
(5,345)

Conversion
(1,856)
–
–
(1,856)

FX impact
92
–
–
92

Change in borrowings and financial liabilities in 2019

Amounts in £‘000
Bond notes
Accrued interest on borrowings
Short-term financing facilities
Total financial liabilities

At 31 
December 
2018
4,703
65
78
4,846

Increase
5,393
34
738
6,165 

Repayment
(2,673)
(63)
(93)
(2,829)

Conversion/
other 
non-cash 
movements
(876)
– 
– 
(876)

FX impact
(191)
(3)
(3) 
(197)

Total
6,356
32
721
7,109

Total
4,703
64
79
4,846

At 31 
December 
2020
–
–
–
–

At 31 
December 
2019
6,356
33
720
7,109

As of 31 December 2020, the Group had repaid or converted all bond notes outstanding at December 2019. During 2020 the main 
operations were as follows:

•  The Vatel bond notes issued in 2017 by Novacyt were repaid in full for an amount of £139,000.

•  The Vatel bond notes issued in 2018 by Novacyt were repaid for an amount of £345,000 and the balance was converted in share 

capital for a total of £1,856,000.

•  The Harbert bond granted to Novacyt UK Holdings in 2019 was repaid in full for an amount of £4,108,000.

In addition, the Group repaid in full its short-term financing facility for an amount of £721,000.

26. BORROWINGS continued
Bond notes
As of 31 December 2019, the Group’s financing was primarily comprised of the following:

Vatel Bonds

•  A convertible bond subscribed by Vatel in the amount of €1.5 million issued on 31 March 2017, with an effective interest rate of 
12.7% for a term of three years. The Vatel Bonds were convertible at the option of Vatel into 1.25 shares for each bond of €1 of 
nominal value only where the Company fails to comply with its payment obligations of the principal or the interest amounts due 
under the loan agreement within 15 days of receipt of a notice of an event of default.

•  A convertible bond subscribed by Vatel in the amount of €4.0 million issued on 29 May 2018, with an effective interest rate of 

8.5% for a term of three years. The Vatel Bonds were convertible at the option of Vatel into 1.429 shares for each bond of €1 of 
nominal value only where the Company fails to comply with its payment obligations of the principal or the interest amounts due 
under the agreement within 15 days of receipt of a notice of an event of default.

•  Both conversion options granted to Vatel have not been recorded in the accounts, as the probability of a default was not 

considered as material.

Harbert Bonds

•  A bond subscribed by Harbert European Growth Capital in the amount of €5.0 million issued on 5 November 2019, with an 

effective interest rate of 13.5% for a term of four years. The Harbert bonds are issued by Novacyt UK Holdings simultaneously 
with warrants giving access to the share capital of Novacyt SA. The number of shares for which the holder of the warrants could 
subscribe, and the subscription price could be either:

 − Subscription for 6,017,192 shares at a subscription price of € 0.0698 per share (i.e. an overall subscription price of €420,000); 

or

 − Subscription at a price of €0.0667 per share for a number of shares equal to:

6,017,192 - [

6,017,192 x (0.0698 – 0.0667)
30 day average of Novacyt share price on exercise date

]

 − The warrants are accounted for as derivative liabilities in “trade and other liabilities”.

Short-term financing facilities

In addition to the bond notes above, the Group financed its short-term working capital needs through convertible notes issued with 
warrants. On 18 April 2019, Novacyt SA entered into an agreement with the Negma Group (“Negma”) under which Negma was 
granted warrants (the “Tranche Warrants”) that gave it the right to subscribe for convertible loan notes issued by Novacyt SA with 
attaching warrants (the “Attaching Warrants”). The Company could issue the loan notes over the subsequent 36 months, in several 
successive tranches representing bond debt in a maximum amount of €5,000,000.

The convertible loan notes (Obligations Convertibles en Actions (“OCA”)) were issued at par, i.e. €2,500 each, with no interest rate, 
and had a maturity of one year from issue. The Company had to redeem unconverted OCAs upon maturity.

The bond debt represented by the OCAs (par value of an OCA) could be converted into shares at the request of the holder, on the 
basis of the following conversion rate: 88% of the lowest of the 15 average daily prices of the Company’s share weighted by volume 
(as reported by Bloomberg) immediately preceding the request for the conversion of the relevant OCA, without it being possible for 
this amount to be lower than the par value of the Company’s share, i.e. 1/15th of a Euro. The OCAs were transferable subject to the 
Company prior written consent.

The number of Attaching Warrants that could be issued upon each issuance of OCAs was that which would be multiplied by the 
exercise price of the equity warrants (determined under the terms set out below). The amount received would be equal to 30% of the 
par value of the OCAs issued, i.e. €655,500 for the first tranche.

The Attaching Warrants would be immediately detached from the OCAs and would be transferable from issue. They could be 
exercised from issue until the 60th month inclusive following their issue date (the “Exercise Period”). Each Attaching Warrant would 
entitle the holder thereof, during the Exercise Period, to subscribe for one new Novacyt SA share.

114

115

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The exercise price of the equity warrants was equal to 115% of the average price of the Novacyt share on the day immediately 
preceding the Warrant exercise request date, giving rise to the issuance of the OCAs from which the Attaching Warrants would be 
detached (or the issue date of the OCAs for the first tranche of OCAs, i.e. 25 April 2019).

The loan agreement offered protection to the Negma Group in the event of the modification by Novacyt SA of the allocation of its 
profits as a result of the issue of preference shares. A similar protection was not afforded to the ordinary Shareholders and therefore 
this would change the relative rights of the Shareholders and warrant holders. As nothing prevented Novacyt SA from issuing 
preference shares, therefore the Attaching Warrants fail the fixed for fixed test and were accounted for as derivative liabilities in the 
line “trade and other liabilities”.

The OCAs and the Attaching Warrants would not be the subject of a request for admission to trading on Alternext Paris and, as such, 
would not be listed.

In accordance with IAS 32, the first tranche of the bond issued on 25 April in the amount of €2,000,000 (tranche 1) breaks down as follows:

•  The conversion option, treated in this case as an embedded derivative under IAS 32, worth €297,955, was recorded at “fair value 

through profit or loss” in current borrowings;

•  The attaching warrants, valued at €236,365 overall, were treated as an embedded derivative were recorded at “fair value through 

profit or loss” in current borrowings; and

•  The residual amount, €1,465,680, was recognised at amortised cost under current financial liabilities.

On 25 April 2019, the Company exercised some of its Tranche Warrants resulting in the issuance of 800 OCAs in a total of 
€2,000,000, an additional 74 OCAs as settlement of issuance fees and 2,979,544 Attaching Warrants.

Between 25 April 2019 and 2 October 2019, the Company had converted 596 OCAs. The remaining 278 OCAs were redeemed by 
anticipation as a result of a supplementary agreement dated 8 November 2019. Besides, the Company and Negma agreed that the 
additional Tranches Warrants in the amount €3,000,000 were cancelled and that the exercise price of each Attaching Warrant was 
changed to €0.20 per share.

As of 31 December 2018, the Group’s financing primarily comprised: 

Kreos Bonds

•  A bond subscribed by Kreos Capital IV Ltd in the amount of €3.5 million issued on 15 July 2015, which was subsequently fully 

repaid in November 2019;

•  A bond subscribed by Kreos Capital V Ltd in the amount of €3 million issued on 12 May 2016, which was subsequently fully 

repaid in November 2019.

Vatel Bonds

•  A convertible bond subscribed by Vatel in the amount of €1.5 million issued on 31 March 2017, with an effective interest rate of 

12.7% for a term of three years; 

•  A convertible bond subscribed by Vatel in the amount of €4.0 million issued on 29 May 2018, with an effective interest rate of 

8.5% for a term of three years; 

•  Both conversion options granted to Vatel have not been recorded in the accounts, as the probability of a default was not 

considered as material.

116

27. LEASE LIABILITIES
The following tables show lease liabilities carried at amortised cost resulting from the application of the IFRS 16 at 1 January 2019.

Maturities

Amounts in £‘000
Lease liabilities short-term
Lease liabilities long-term
Total lease liabilities

Year ended 
31 December 
2020
414
1,964
2,378

 Year ended 
31 December 
2019 
229
2,012
2,241

 Year ended 
31 December 
2018 
–
–
–

Change in lease liabilities in 2020 and 2019

Amounts in £’000
Changes in 2019
Changes in 2020

Adoption of 
IFRS 16
2,333
–

Business 
Combinations 
Impact
–
73

Opening
–
2,241

Repayment
(183)
(303)

Non-cash 
movements
91
367

Closing
2,241
2,378

28. RECONCILIATION OF THE MOVEMENTS OF THE BORROWINGS AND LEASE 
LIABILITIES WITH THE STATEMENT OF CASH-FLOWS
Repayment of borrowings and lease liabilities in 2020
Note 26 – Borrowings and note 27 – Lease liabilities
Change in borrowings in 2020: repayment of bond notes
Change in borrowings in 2020: repayment of short-term financing facilities
Change in lease liabilities in 2020: repayment 
Total repayments in 2020 as per notes 26 and 27

£’000
(4,592)
(720)
(303)
(5,615)

Statement of cash flows for the year 2020
Cash used in financing activities: repayment of borrowings
Cash used in financing activities: repayment of lease liabilities
Cash used in financing activities: variation of other short-term financing facilities
Total repayments as per the statement of cash flows

Repayment of borrowings and lease liabilities in 2019
Note 26 – Borrowings and note 27 – Lease liabilities
Change in borrowings in 2019: repayment of bond notes
Change in borrowings in 2019: repayment of short-term financing facilities
Change in lease liabilities in 2019: repayment 
Issuance of Negma conversion options 
Total repayments in 2019 as per notes 26 and 27

Statement of cash flows for the year 2019
Cash used in financing activities: repayment of borrowings
Cash used in financing activities: repayment of lease liabilities
Cash used in financing activities: variation of other short-term financing facilities
Total repayments as per the statement of cash flows

(4,592)
(303)
(720)
(5,615)

£’000
(2,673)
(93)
(183)
(83)
(3,032)

(2,756)
(183)
(93)
(3,032)

117

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Novacyt Group Annual Report and Accounts for the year ended 31 December 2020Strategic ReportBusiness OverviewOur GovernanceFinancial StatementsCompany InformationNotes to the annual accounts continuedfor the years ended 31 December 2020 and 31 December 201928. RECONCILIATION OF THE MOVEMENTS OF THE BORROWINGS AND LEASE 
LIABILITIES WITH THE STATEMENT OF CASH-FLOWS continued
Proceeds from borrowings in 2019
Note 26 – Borrowings 
Change in borrowings in 2019: increase of bond notes
Change in borrowings in 2019: increase of short-term financing facilities
Other cash movement: issuance of Negma conversion options
Other cash movement: issuance of Negma warrants
Total proceeds in 2019 as per notes 26 and 27

£’000
5,393
738
261
207
6,599

Statement of cash flows for the year 2019
Cash from financing activities: issue of borrowings and bond notes
Cash from financing activities: variation of other short-term financing facilities
Total proceeds as per the statement of cash flows

29. CONTINGENT CONSIDERATION 

Amounts in £‘000
Contingent consideration short-term
Contingent consideration long-term
Total contingent consideration

5,922
677
6,599

Year ended 
31 December 
2020
1,022
812
1,834

 Year ended 
31 December 
2019 
–
–
–

 Year ended 
31 December 
2018 
1,415
–
1,415

At 31 December 2020, the contingent consideration relates to the acquisition of IT-IS International by Novacyt UK Holdings Ltd (see 
note 40). It will be settled in two payment tranches, which are due September 2021 and 2022.

At 31 December 2018, the contingent consideration related to the acquisition of Primerdesign and the Asset Purchase Agreement of 
the Omega Infectious Diseases business. The Group settled both debts in 2019.

30. PROVISIONS
The nature of and changes in provisions for risks and charges for the period from 1 January 2020 to 31 December 2020 are as 
follows:

Amounts in £‘000
Provisions for restoration of premises
Long-term management incentive plan
Provisions long-term
Provision for litigation
Provisions for product warranty
Provisions short-term

At  
1 January 
2020
192
13
205
43
–
43

Business 
Combinations 
Impact
13
–
13
–
35
35

Reduction
–
(19,018)
(19,018)
–
–
–

Change in 
exchange 
rates
–
(1)
(1)
3
–
3

At  
31 December 
2020
242
–
242
68
19,788
19,856

Increase
37
19,006
19,043
22
19,753
19,775

30. PROVISIONS continued
The nature of and changes in provisions for risks and charges for the period from 1 January 2019 to 31 December 2019 are as 
follows.

Amounts in £‘000
Provisions for restoration of premises
Long-term management incentive plan
Provisions long-term
Provision for litigation
Provisions short-term

Provisions chiefly cover: 

•  Risks related to litigations with personnel;

At  
1 January 
2019
133
18
151
90
90

Increase
6
 –
6
–
–

Reduction
(23)
(5)
(28)
(44)
(44)

Adoption of 
IFRS 16
76
 –
76
 –
 –

Change in 
exchange 
rates
–
– 
– 
(3) 
(3)

At 31 
December 
2019
192
13 
205
43 
43 

•  The restoration expenses of the premises as per the lease agreements; and

•  Product assurance warranties.

The provisions for the restoration of the premises is an estimation of the cash payable to cover dilapidations at the end of the rental 
periods, thus at the following dates: 

•  Lab21 Healthcare Ltd: August 2025

•  Microgen Bioproducts Ltd: May 2032 

•  Primerdesign Ltd: November 2025

•  IT-IS International Ltd: September 2022 and December 2023, as there are two sites that do not have co-terminus leases

The provision for litigations may generate a cash payment during 2021. 

The provision for product assurance warranties has increased significantly in the year due to higher sales and the notification of a 
product warranty claim after the year end (see note 50).

The details for the long-term management incentive plan are shown in note 3, and the liability crystalised in November 2020 and the 
remaining costs are shown against other liabilities.

118

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Amounts in £‘000
Trade payables
Accrued invoices
Social security liabilities
Tax liabilities
Other liabilities
Options classified as liabilities
Total trade and other liabilities

 Year ended 
31 December 
2020 
5,228 
8,016 
1,082 
16,831 
5,627 
– 
36,784 

 Year ended 
31 December 
2019 
1,786 
732 
404 
122 
31 
845 
3,920 

 Year ended 
31 December 
2018 
2,497 
1,072 
269 
253 
94 
5 
4,190 

Trade payables and accrued invoices have increased significantly in line with increased revenue. In addition, the improved liquidity 
position has meant that credit facilities have been secured with many suppliers who previously did not offer such terms.

The 2020 “tax liability” predominantly relates to Value Added Tax (“VAT”) payable to HMRC in the UK covering the months of 
November and December.

The 2020 “other liabilities” balance relates to the second tranche of the LTIP payment that is due to be paid in November 2021.

“Options classified as liabilities” in 2019 relate mainly to the Company’s equity warrants granted to Harbert European Growth Capital 
in connection with the subscription of the €5,000,000 bond issued by Novacyt UK Holdings and to the equity warrants attached to 
the OCABSAs subscribed by Negma.

32. TAX LIABILITIES
The balance of £15,116,000 at 31 December 2020 (2019: £nil; 2018: £nil) reflects the UK corporation tax liability of the Group. The 
amount reflects the tax due at the full UK rate (19%) on taxable profits, although in due course, if patents are granted and a Patent 
Box claim be made, future taxable profits should be taxable at a much lower rate.

33. OTHER CURRENT LIABILITIES

Amounts in £‘000
Deferred income and advance payments received from customers
Total other current liabilities

The balances above relate to customer payments in advance of receiving the products.

34. OTHER LIABILITIES LONG-TERM

Amounts in £‘000
Share-based payment benefits – LTIP, long-term
Total other liabilities long-term

 Year ended 
31 December 
2020 
 950 
 950 

 Year ended 
31 December 
2019 
 505 
 505 

 Year ended 
31 December 
2018 
 341 
 341 

 Year ended 
31 December 
2020 
5,606 
5,606

 Year ended 
31 December 
2019 
–
–

 Year ended 
31 December 
2018 
–
–

The 2020 “other liabilities long-term” balance relates to the third tranche of the LTIP payment that is due to be paid in November 2022.

35. SHARE CAPITAL
As of 1 January 2019, the Company’s share capital of €2,510,956.06 was divided into 37,664,341 shares with a par value of 1/15th 
of a Euro each. 

The transactions on share capital from this date are summarised below:

•  On 26 April 2019, the Company completed a capital increase by conversion of one convertible bond Negma from €2,510,956.06 

to €2,511,997.73 through the issue of 15,625 shares at a price of €0.160 per share, with a share premium of €1,458.33. 

•  On 2 May 2019, the Company completed a capital increase by conversion of seven convertible bonds Negma from 

€2,511,997.73 to €2,519,775.46 through the issue of 116,666 shares at a price of €0.150 per share, with a share premium of 
€9,722.27.

•  On 14 May 2019, the Company completed a capital increase by conversion of 33 convertible bonds Negma from €2,519,775.46 

to €2,559,061.13 through the issue of 589,285 shares at a price of €0.140 per share, with a share premium of €43,214.33.

•  On 16 May 2019, the Company completed a capital increase by conversion of 27 convertible bonds Negma from €2,559,061.13 

to €2,596,561.06 through the issue of 562,499 shares at a price of €0.120 per share, with a share premium of €30,000.07.

•  On 12 June 2019, the Company completed a capital increase by conversion of five convertible bonds Negma from €2,596,561.06 

to €2,605,820.26 through the issue of 138,888 shares at a price of €0.090 per share, with a share premium of €3,240.80.

•  On 18 June 2019, the Company completed a capital increase by conversion of 17 convertible bonds Negma from €2,605,820.26 

to €2,637,301.73 through the issue of 472,222 shares at a price of €0.090 per share, with a share premium of €11,018.53.

•  On 19 June 2019, the Company completed a capital increase by conversion of 22 convertible bonds Negma from €2,637,301.73 

to €2,678,042.46 through the issue of 611,111 shares at a price of €0.090 per share, with a share premium of €14,259.27.

•  On 21 June 2019, the Company completed a capital increase by conversion of seven convertible bonds Negma from 

€2,678,042.46 to €2,691,005.39 through the issue of 194,444 shares at a price of €0.090 per share, with a share premium of 
€4,537.07.

•  On 24 June 2019, the Company completed a capital increase by conversion of eight convertible bonds Negma from 

€2,691,005.39 to €2,705,820.19 through the issue of 222,222 shares at a price of €0.090 per share, with a share premium of 
€5,185.20.

•  On 28 June 2019, the Company completed a capital increase by conversion of two convertible bonds Negma from €2,705,820.19 

to €2,709,986.86 through the issue of 62,500 shares at a price of €0.080 per share, with a share premium of €833.33.

•  On 8 July 2019, the Company completed a capital increase by conversion of one convertible bond Negma from €2,709,986.86 to 

€2,712,367.79 through the issue of 35,714 shares at a price of €0.070 per share, with a share premium of €119.07.

•  On 15 July 2019, the Company completed a capital increase by conversion of 30 convertible bonds Negma from €2,712,367.79 

to €2,783,796.32 through the issue of 1,071,428 shares at a price of €0.070 per share, with a share premium of €3,571.47.

•  On 16 July 2019, the Company completed a capital increase by conversion of ten convertible bonds Negma from €2,783,796.32 

to €2,807,605.79 through the issue of 357,142 shares at a price of €0.070 per share, with a share premium of €1,190.53.

•  On 1 August 2019, the Company completed a capital increase by conversion of 100 convertible bonds Negma from 

€2,807,605.79 to €3,057,855.99 through the issue of 3,753,753 shares at a price of €0.070 per share, with a share premium of 
-€250.20.

•  On 6 August 2019, the Company completed a capital increase by conversion of 51 convertible bonds Negma from €3,057,855.99 

to €3,185,483.59 through the issue of 1,914,414 shares at a price of €0.070 per share, with a share premium of -€127.60.

•  On 12 August 2019, the Company completed a capital increase by conversion of 51 convertible bonds Negma from 

€3,185,483.59 to €3,312,983.59 through the issue of 1,912,500 shares at a price of €0.070 per share, with no share premium.

•  On 23 August 2019, the Company completed a capital increase by conversion of 40 convertible bonds Negma from 

€3,312,983.59 to €3,412,983.59 through the issue of 1,500,000 shares at a price of €0.070 per share, with no share premium.

•  On 28 August 2019, the Company completed a capital increase by conversion of 60 convertible bonds Negma from 

€3,412,983.59 to €3,562,983.59 through the issue of 2,250,000 shares at a price of €0.070 per share, with no share premium.

•  On 11 September 2019, the Company completed a capital increase by conversion of 20 convertible bonds Negma from 

€3,562,983.59 to €3,612,983.59 through the issue of 750,000 shares at a price of €0.070 per share, with no share premium.

120

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•  On 12 September 2019, the Company completed a capital increase by conversion of 18 convertible bonds Negma from 

€3,612,983.59 to €3,657,983.59 through the issue of 675,000 shares at a price of €0.070 per share, with no share premium.

•  On 18 September 2019, the Company completed a capital increase by conversion of 12 convertible bonds Negma from 

€3,657,983.59 to €3,687,983.59 through the issue of 450,000 shares at a price of €0.070 per share, with no share premium.

•  On 23 September 2019, the Company completed a capital increase by conversion of ten convertible bonds Negma from 

€3,687,983.59 to €3,712,983.59 through the issue of 375,000 shares at a price of €0.070 per share, with no share premium.

•  On 25 September 2019, the Company completed a capital increase by conversion of 38 convertible bonds Negma from 

€3,712,983.59 to €3,807,983.59 through the issue of 1,425,000 shares at a price of €0.070 per share, with no share premium.

•  On 27 September 2019, the Company completed a capital increase by conversion of 18 convertible bonds Negma from 

€3,807,983.59 to €3,852,983.59 through the issue of 675,000 shares at a price of €0.070 per share, with no share premium.

•  On 2 October 2019, the Company completed a capital increase by conversion of eight convertible bonds Negma from 

€3,852,983.59 to €3,872,983.59 through the issue of 300,000 shares at a price of €0.070 per share, with no share premium.

•  On 31 January 2020, the Company completed a capital increase resulting from the exercise of 1,679,544 Negma warrants from 
€3,872,983.59 to €3,984,953.20, through the issue of 1,679,544 shares at a price of €0.070 per share with a share premium of 
€223,939.20.

•  On 17 February 2020, the Company completed a capital increase resulting from the exercise of 228,541 Yorkville warrants from 
€3,984,953.20 to €4,000,189.27, through the issue of 228,541 shares at a price of €0.070 per share with a share premium of 
€200,963.72.

•  On 17 February 2020, the Company completed a capital increase resulting from the exercise of 886,632 Primerdesign warrants 
from €4,000,189.27 to €4,059,298.07, through the issue of 886,632 shares at a price of €0.070 per share with a share premium 
of €969,384.32.

•  On 18 February 2020, the Company completed a capital increase resulting from the exercise of 113,368 Primerdesign warrants 
from €4,059,298.07 to €4,066,855.94, through the issue of 113,368 shares at a price of €0.070 per share with a share premium 
of €123,949.01.

•  On 18 February 2020, the Company completed a capital increase resulting from the exercise of 6,017,192 Harbert warrants from 
€4,066,855.94 to €4,468,002.06, through the issue of 6,017,192 shares at a price of €0.070 per share with a share premium of 
€18,853.87.

•  On 18 February 2020, the Company completed a capital increase resulting from the exercise of 300,000 Yorkville warrants from 
€4,468,002.06 to €4,488,002.06, through the issue of 300,000 shares at a price of €0.070 per share with a share premium of 
€263,800.00.

•  On 18 February 2020, the Company completed a capital increase resulting from the exercise of 353,536 Kreos warrants from 
€4,488,002.06 to €4,511,571.13, through the issue of 353,536 shares at a price of €0.070 per share with a share premium of 
€489,058.13.

•  On 3 June 2020, the Company completed a capital increase by conversion of 2,066,257 Vatel convertible bonds from 

€4,511,571.13 to €4,708,416.54 through the issue of 2,952,681 shares at a price of €0.070 per share, with a share premium of 
€1,869,411.09.

At 1 January 2019
Capital increase by conversion of OCABSA
At 31 December 2019
Capital increase by exercise of warrants
Capital increase by conversion of bonds
At 31 December 2020

Amount of 
share capital 
in £‘000

Amount of 
share capital 
in €‘000 

Unit value per 
share in €

Number of 
shares issued

2,117
1,194
3,311
567
175
4,053

2,511
1,362
3,873
638
197
4,708

0.07
0.07
0.07
0.07
0.07
0.07

37,664,341
20,430,413
58,094,754
9,578,813
2,952,681
70,626,248

As of 31 December 2020, the Company’s share capital of €4,708,416.54 was divided into 70,626,248 shares with a par value of 
1/15th of a Euro each. 

122

The Company’s share capital consists of one class of share. All outstanding shares have been subscribed, called and paid.

36. SHARE PREMIUM ACCOUNT
Amounts in £‘000
Balance at 1 January 2019
Premium arising on issue of equity shares
Expenses of issue of equity shares
Balance at 31 December 2019
Premium arising on issue of equity shares
Expenses of issue of equity shares
Balance at 31 December 2020

37. OTHER RESERVES
Amounts in £‘000
Balance at 1 January 2019
Translation differences
Balance at 31 December 2019
Translation differences
Balance at 31 December 2020

38. EQUITY RESERVE
Amounts in £‘000
Balance at 1 January 2019
Conversion of the OCABSA Negma 
Balance at 31 December 2019
Conversion Vatel bonds
Exercise Negma warrants
Exercise Harbert European Growth Capital warrants
Exercise Primerdesign warrants
Balance at 31 December 2020

This reserve represents the equity component of warrants and loans.

39. RETAINED EARNINGS/LOSSES
Amounts in £‘000
Balance at 1 January 2019
Loss for the year
Other variations
Balance at 31 December 2019
Profit for the year
Other variations
Balance at 31 December 2020

 47,207 
 112 
(320) 
 46,999 
 3,697 
(25) 
 50,671 

(4,395) 
 2,471 
(1,924) 
(112) 
(2,036) 

 355 
(19)
 336 
 19 
 103 
 693 
 4 
 1,155 

(26,981) 
(5,749) 
(3,389) 
(36,119) 
 132,423 
612 
 96,916 

123

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40. BUSINESS COMBINATIONS
Acquisition of IT-IS International Ltd
On 15 October 2020, Novacyt UK Holdings Ltd completed the purchase of the entire share capital of IT-IS International Ltd, a 
company incorporated in England and Wales. The company specialises in the development and manufacturing of PCR diagnostic 
instruments for the life sciences and food testing industry.

40. BUSINESS COMBINATIONS continued
The table below presents the Group income statement for the 12 months period ended on 31 December 2020 as if the acquisition of 
IT-IS International had been completed on 1 January 2020.

The purchase price was £13,387,000, broken down as follows:

Cash disbursed
Deferred consideration for reaching a target turnover in year one
Deferred consideration for reaching a target turnover in year two
Total purchase price

The fair value of the assets acquired and the liabilities assumed are as follows: 

Net property, plant and equipment
Trademark
Customer relationships
Inventory
Clients and other receivables
Suppliers and other creditors
Deferred tax on assets acquired
Cash acquired
Fair value of assets acquired and liabilities assumed

Goodwill

£11,564,000
£1,016,000
£807,000
£13,387,000

£108,000
£843,000
£1,366,000
£1,774,000
£424,000
(£4,680,000)
(£591,000)
£4,706,000
£3,950,000

£9,437,000

Amounts in £’000
Revenue 
Cost of sales
Gross profit
Sales, marketing and distribution expenses
Research and development expenses
General and administrative expenses
Governmental subsidies
Operating profit before exceptional items
Costs related to acquisitions
Other operating expenses
Operating profit after exceptional items
Financial income
Financial expenses
Profit before tax
Tax expense
Profit after tax
Profit after tax attributable to owners of the Company

The table above shows how the goodwill figure of £9,437,000 is arrived at after allocating the purchase price across all the assets 
and liabilities acquired. The residual goodwill arising from the acquisition reflects the future growth expected to be driven by new and 
existing customers, the value of the workforce, patents and know-how.

The value of “customer relationships” was determined by discounting the additional margin generated by customers after 
remuneration of the contributing assets.

The value of the trademark was determined by discounting the cash flows that could be generated by licensing the trademark, 
estimated as a percentage of revenue derived from information available on comparable assets.

IFRS 3 provides for a period of 12 months from acquisition to complete the identification and measurement of the fair value of assets 
acquired and liabilities assumed. This means that the gross amount of goodwill is subject to adjustment until October 2021.

Goodwill is a residual component calculated as the difference between the purchase price for the acquisition of control and the fair 
value of the assets acquired and liabilities assumed. It includes unrecognised assets such as the value of the personnel and know-
how of the acquiree. 

The acquisition costs amounted to £187,000. They are included on the statement of comprehensive income in the year ended 31 
December 2020 as “acquisition related expenses”; see note 11.

IT-IS International contributed £1,077,000 to consolidated revenue in the year ended 31 December 2020 between its consolidation 
on 15 October 2020 and 31 December 2020.

If the acquisition of the IT-IS International shares were deemed to have been completed on 1 January 2020, the opening date of 
the Group’s 2020 financial year, consolidated Group revenue would have amounted to £279,781,000 and net profit attributable to 
owners of the Company of £132,219,000.

Year ended 
31 December 
2020 
Pro forma 
279,781
(66,961)
212,820
(4,867)
(1,929)
(31,484)
(3)
174,537
(187)
(7,215)
167,135
85
(2,357)
164,863
(32,644)
132,219
132,219

124

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Novacyt had begun the formal sale process for the NOVAprep (Cytology business) and Cambridge Clinical Labs businesses in late 
2018. The Cambridge Clinical Lab business was a non-core service business and did not fit in with the long-term high-margin growth 
strategy for the Group. NOVAprep was being sold as it continued to be loss making and was a drain on working capital.

The NOVAprep business was sold in December 2019 via an Asset Purchase Agreement. The Cambridge Clinical Labs business was 
sold in July 2019 through the sale of the shares of Lab21 Ltd.

The assets and liabilities available for sale were transferred to the lines “assets classified as held for sale” and “liabilities directly 
associated with assets classified as held for sale” in the 2018 financial results. The value of these assets and liabilities at December 
2018 are presented in the table below:

Amounts in £‘000
Goodwill
Other intangible assets
Property, plant and equipment
Non-current assets
Inventories and work in progress
Trade and other receivables
Current assets
Total assets classified as held for sale
Trade and other liabilities
Total current liabilities
Provisions - long-term
Total non-current liabilities
Total liabilities directly associated with assets classified as held for sale

Cambridge 
Clinical Labs
584
–
3
587
22
44
66
653
39
39
6
6
45

NOVAprep
–
748
253
1,001
414
–
414
1,415
16
16
16
16
32

Total
584
748
256
1,588
436
44
480
2,068
55
55
22
22
77

In accordance with IFRS 5, the net result of the NOVAprep business was transferred to the line “loss from discontinued operations”.

The table below presents the detail of the loss generated by this business in 2018 and 2019.

Amounts in £‘000
Revenue
Cost of sales
Gross profit
Sales, marketing and distribution expenses
Research and development expenses
General and administrative expenses
Governmental subsidies
Operating loss before exceptional items
Other operating expenses
Operating loss after exceptional items
Loss before tax
Tax (expense) / income
Loss after tax from discontinued operations

Year ended 
31 December 
2019
1,172 
(668) 
504 
(772) 
(137) 
(1,676) 
– 
(2,081) 
(249) 
(2,330) 
(2,330) 

Year ended 
31 December 
2018
862 
(636) 
226 
(1,035) 
(167) 
(1,383) 
78 
(2,281) 
(42) 
(2,323) 
(2,323) 

 –

–

(2,330) 

(2,323) 

42. NOTES TO THE CASH FLOW STATEMENT

Amounts in £‘000
Profit/(loss) for the year
Profit/(loss) from the discontinued activities
Profit/(loss) from the continuing operations
Adjustments for:
Depreciation, amortisation, impairment loss and provisions
Product warranty provision
Unwinding of discount on contingent consideration
(Increase)/decrease of fair value
Losses/(gains) on disposal of fixed assets
Income tax charge
Operating cash flows before movements of working capital
(Increase)/decrease in inventories
(Increase)/decrease in receivables
Increase/(decrease) in payables
Cash used in operations
Income taxes (paid)/received
Finance costs
Net cash used in operating activities
Operating cash flows from the discontinued activities
Operating cash flows from the continuing operations

Year ended 
31 December 
2020
132,423
–
132,423

Year ended 
31 December 
2019
(5,749)
(2,330)
(3,419)

8,196
19,753
(114)
–
407
32,751
193,416
(25,966)
(80,773)
34,838
121,515
(20,574)
2,035
102,976
–
102,976

1,589
–
81
657
300
–
(3,123)
371
1,533
(752)
(1,971)
72
958
(941)
(1,124)
183

43. LEASES
In application of IFRS 16 as from 1 January 2019, the Group has recognised on the statement of financial position some “right-of-
use” assets and lease liabilities. 

Novacyt S.A.
Novacyt SA rents a small office in Vélizy, on a rolling 12-month basis.

Primerdesign Limited
A lease exists for the York House site which is used for office, storage, and laboratory purposes. The annual charge for the site (with 
service charges) is now £176,813 per annum, with all leases running to November 2025.

In November 2020, the company took out a new lease at a nearby site called Unit A, primarily for storage purposes. The lease runs 
to November 2022 with the first six months incurring a charge of £72,000, and then an annual charge of £97,833.

Microgen Bioproducts Ltd
A lease exists at Watchmoor Park, which has a mixed use for office, storage, and laboratory purposes. This commenced in May 
2017 and will run until May 2032. There are rent review clauses in May 2022 and 2027. The annual charge for the site is £173,173 
per annum (including service charges).

Lab21 Healthcare Ltd
A lease existed for the Bridport site which was being used for manufacturing, storage, and laboratory purposes. The annual charge 
for the site was £42,940 per annum. In 2020 all manufacturing activities were moved from the Bridport site to Watchmoor Park and 
in February 2021 the company terminated the Bridport lease and settled all agreed liabilities.

The lease for the Axminster site, which ran until October 2019, was not renewed.

126

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IT-IS International Ltd
A lease exists at units 1, 3 and 4 Wainstones Court, which has a mixed use for office, storage, and production purposes. This 
commenced in October 2019 and will run until September 2022. The annual charge for the site is £31,500 per annum (including 
service charges).

44. FINANCIAL INSTRUMENTS continued
Significant accounting policies
Details of the significant accounting policies and methods adopted (including the criteria for recognition, the basis of measurement 
and the bases for recognition of income and expenses) for each class of financial asset, financial liability and equity instrument are 
disclosed in note 3.

In September 2020, the company took out a new 12-month lease at a nearby site called Pulrose House for production purposes. 
The annual charge for the site is £17,000 per annum.

Categories of financial instruments

In December 2020, the company took out a new lease at a nearby site called MMC House, for mixed use of office, storage and 
production purposes. The lease runs to December 2023 with an annual charge of £75,000 (including service charges).

The table below presents the impacts of the leases in the consolidated income and cash flow statements of the financial years 2020 
and 2019:

Amounts in £’000
Interest expense on lease liabilities
Cash outflows for leases accounted for as per IFRS 16
Expenses related to short-term and low-value leases
Total cash outflows for leases

At 31 
December 
2020
184
487
252
739

At 31 
December 
2019
174
358
88
446

44. FINANCIAL INSTRUMENTS
Capital risk management
The Group manages its capital to ensure that entities in the Group will be able to continue as a going concern whilst maximising 
the return to Shareholders through the optimisation of debt and equity balances. The Group’s overall strategy is to ensure there is 
sufficient working capital to optimise the performance of the business.

The capital structure of the Group consists of net debt (borrowings disclosed in note 26 after deducting cash and cash equivalents) 
and equity of the Group (comprising issued capital, reserves and retained losses in notes 35 to 39). 

The Group is not subject to any externally imposed capital requirements.

The Group’s focus is on cash management and this is reviewed on a regular basis by the Group Finance Director and the Chief 
Financial Officer. The funding mix of the business is reviewed and managed regularly by the Chief Financial Officer and the Chief 
Executive Officer.

Amounts in £‘000
Financial assets
Cash and cash equivalents
Loans and receivables
Financial liabilities
Fair value through profit and loss
Amortised cost

Year ended 
31 December 
2020

Year ended 
31 December 
2019

Year ended 
31 December 
2018

 91,765 
 79,396 

 1,542 
 1,721 

(1,834) 
 21,249 

 845 
 12,130 

 1,021 
 3,284 

 5 
 9,924 

Financial risk management objectives
The Group’s finance function is responsible for managing the financial risks relating to the running of the business. These risks include 
market risk (including currency risk, interest rate risk and price risk), credit risk and liquidity risk.

If a material risk is identified then the Group would look to mitigate that risk through the appropriate measure, such as hedging 
against currency fluctuations.

The Group does not use complex derivative financial instruments to reduce its economic risk exposures.

Market risk
The Group’s activities expose it primarily to the financial risks of changes in foreign currency exchange rates. 

There has been no change to the Group’s exposure to market risks or the way these risks are managed and measured.

Foreign currency risk management
The Group undertakes transactions denominated in foreign currencies; consequently, exposures to exchange rate fluctuations arise. 
Exchange rate exposures are not managed utilising forward foreign exchange contracts.

The carrying amounts of the Group’s foreign currency denominated monetary assets and monetary liabilities at the reporting date are 
as follows:

Gearing ratio
The gearing ratio at the year end is as follows:

Amounts in £‘000
Debt
Cash and cash equivalents
Net (cash)/debt
Equity
Net (cash)/debt to equity ratio

Year ended 
31 December 
2020
 2,378 
 91,765 
(89,387) 
 150,710 
(59%)

Year ended 
31 December 
2019
 9,350 
 1,542 
 7,808 
 12,462 
63%

Year ended 
31 December 
2018
 4,846 
 1,021 
 3,825 
 18,159 
21%

Amounts in £‘000
Assets
Liabilities
Net exposure

Debt is defined as long-term and short-term borrowings and lease liabilities (excluding derivatives and financial guarantee contracts) 
as detailed in notes 26 and 27. 

For the year ended 31 December 2020, debt in the table above relates to the leases’ liability as per IFRS 16, but for the year ended 
31 December 2018, debt in the table above does not include the leases’ liability as per IFRS 16.

Equity includes all capital, premiums and reserves of the Group that are managed as capital.

Assets and liabilities denominated in EUR
Year ended 
31 December 
2020
5,419
(1,995)
3,424

Year ended 
31 December 
2019
1,869
(4,459)
(2,590)

Year ended 
31 December 
2018
2,497
(6,112)
(3,615)

Assets and liabilities denominated in USD
Year ended 
31 December 
2020
6,068
(5)
6,063

Year ended 
31 December 
2019
1,083
(417)
577

Year ended 
31 December 
2018
1,680
(291)
1,389

128

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44. FINANCIAL INSTRUMENTS continued
Foreign currency sensitivity analysis
The Group is mainly exposed to the Euro and US Dollar currencies, used in all segments.

The following table details the Group’s sensitivity to a 5% increase and decrease in GBP against the relevant foreign currencies. 5% 
represents management’s assessment of the reasonably possible change in foreign exchange rates. The sensitivity analysis includes 
only outstanding foreign currency denominated monetary items and adjusts their translation at the period end for a 5% change in 
foreign currency rates. The sensitivity analysis includes external loans as well as loans to foreign operations within the Group where 
the denomination of the loan is in a currency other than the currency of the lender or the borrower. A positive number below indicates 
an increase in profit and other equity. 

Net exposure

Amounts in £‘000
EUR
Conversion rate
Impact GBP strengthening : FX + 5 %
Impact GBP weakening : FX - 5 %
USD
Conversion rate
Impact GBP strengthening : FX + 5 %
Impact GBP weakening : FX - 5 %
Interest rate risk management
The Group borrows funds at fixed interest rate and therefore it is not exposed to significant interest rate risk.

Year ended 
31 December 
2020
3,424
0.90472
171
(171)
6,063
1.35772
(289)
319

Year ended 
31 December 
2019

(2,590)
0.85391
(793)
(1,149)
577
1.11998
(27)
30

Year ended 
31 December 
2018

(3,615)
0.90171
(619)
(1,065)
1,389
1.14430
(66)
73

Credit risk management
Credit risk refers to the risk that a counterparty will default on its contractual obligations resulting in financial loss to the Group. The 
Group has adopted a policy of only dealing with creditworthy counterparties and obtaining sufficient collateral where appropriate, as a 
means of mitigating the risk of financial loss from defaults. The Group uses publicly available financial information and its own trading 
records to rate its major customers’ risk levels. The Group’s exposure and the credit ratings of its counterparties are continuously 
monitored and the aggregate value of transactions concluded is spread amongst approved counterparties.

The Group uses debt collection agencies and government-backed schemes to collect difficult aged debts as a last resort.

Trade receivables consist of a large number of customers, spread across diverse geographical areas. Ongoing credit evaluation is 
performed on the financial condition of accounts receivable and, where appropriate, credit guarantee insurance cover is purchased.

The credit risk on liquid funds is limited because the counterparties are banks with high credit ratings assigned by international credit-
rating agencies. 

The carrying amount of the financial assets recorded in the historical financial information, which is net of impairment losses, 
represents the Group’s maximum exposure to credit risk as no collateral or other credit enhancements are held.

Liquidity risk management
Ultimate responsibility for liquidity risk management rests with the Board of Directors, which has established an appropriate liquidity 
risk management framework for the management of the Group’s short, medium and long-term funding and liquidity management 
requirements. The Group manages liquidity risk by maintaining adequate reserves, banking facilities and reserve borrowing facilities, 
by continuously monitoring forecast and actual cash flows, and by matching the maturity profiles of financial assets and liabilities.

44. FINANCIAL INSTRUMENTS continued
Liquidity and interest risk tables
The following tables detail the Group’s remaining contractual maturity for its non-derivative financial liabilities with agreed repayment 
periods. The tables have been drawn up based on the undiscounted cash flows of financial liabilities based on the earliest date on 
which the Group can be required to pay. The table includes both interest and principal cash flows. The contractual maturity is based 
on the earliest date when the Group may be required to pay.

31 December 2020
Variable interest rate instruments
Fixed interest rate instruments
31 December 2019
Variable interest rate instruments
Fixed interest rate instruments

Effective 
interest rate
%

Less than  
1 month
£‘000

1-3 months
£‘000

3 months to 
1 year
£‘000

1-5 years
£‘000

5+ years
£‘000

7.5

10.4

–
58

–
348

–
103

–
427

–
411

–
1,707

–
1,566

–
9,041

–
1,224

–
1,926

Total
£‘000

–
3,362

–
13,451

The following table details the Group’s expected maturity for its non-derivative financial assets. The tables below have been drawn 
up based on the undiscounted contractual maturities of the financial assets including any interest that will be earned on those assets. 
The inclusion of information on non-derivative financial assets is necessary to understand the Group’s liquidity risk management as 
the liquidity is managed on a net asset and liability basis.

31 December 2020
Non-interest bearing
31 December 2019
Non-interest bearing

Effective 
interest rate
%

Less than  
1 month
£‘000

1-3 months
£‘000

3 months to 1 
year
£‘000

1-5 years
£‘000

Total
£‘000

–

–

169,558

1,467

74

234

171,360

 2,499

 383

 193

 378

 3,453 

Fair value measurements
The information set out below provides information about how the Group determines fair values of various financial assets and 
financial liabilities.

The following table provides an analysis of financial instruments that are measured subsequent to initial recognition at fair value, 
grouped into Levels 1 to 3 based on the degree to which the fair value is observable:

•  Level 1 fair value measurements are those derived from quoted prices (unadjusted) in active markets for identical assets or 

liabilities;

•  Level 2 fair value measurements are those derived from inputs other than quoted prices included within Level 1 that are 

observable for the asset or liability, either directly (i.e. as prices) or indirectly (i.e. derived from prices); and

•  Level 3 fair value measurements are those derived from valuation techniques that include inputs for the asset or liability that are not 

based on observable market data (unobservable inputs).

130

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Fair value of the Group’s financial assets and financial liabilities that are measured at fair value on 
a recurring basis
Some of the Group’s financial assets and financial liabilities are measured at fair value at the end of each reporting period. The 
following table gives information about how the fair values of these financial assets and financial liabilities are determined (in particular, 
the valuation technique(s) and inputs used).

Significant 
unobservable input(s) 

Relationship of unobservable 
inputs to fair value 

Financial assets/ 
financial liabilities
1) Contingent 

consideration 

Fair value as at £’000
31/12/20 31/12/19 31/12/18
1,415
–
1,834

Fair value 
hierarchy 
 2 

2) Trade and other 

–

3

5

2

payables: Options 
classified as 
liabilities – Warrant 
Primerdesign

 Valuation technique(s) 
and key input(s) 
Payments due 
in September 
2021 and 2022, 
estimated 
according to the 
probability of 
payment
Monte Carlo 
simulation model 

Expected volatility 
of 84.3% used for 
December 2019

3) Trade and other 

–

666

–

 2

payables: Options 
classified as liabilities 
– Warrant Harbert

Monte Carlo 
simulation model 

Expected volatility 
of 65.9% used for 
December 2019

4) Trade and other 

–

176

–

2

payables: Options 
classified as liabilities 
– warrants Negma

Black-Scholes 
model

Expected volatility 
of 59.7% used for 
December 2019

If the expected volatility 
was 5% higher or lower 
while other variables 
were held constant, the 
carrying amount would 
respectively increase by 
£5,000 and decrease by 
£3,000 as at December 
2019. 
If the expected volatility 
was 5% higher or lower 
while other variables 
were held constant, the 
carrying amount would 
respectively increase by 
£320,000 and decrease 
by £286,000 as at 
December 2019. 

44. FINANCIAL INSTRUMENTS continued
Fair value measurements recognised in the statement of financial position

Amounts in £‘000
Financial liabilities at FVTPL
Debts from the acquisition of shares
Total liabilities at FVTPL

Amounts in £‘000
Financial liabilities at FVTPL
Derivatives financial liabilities
Total liabilities at FVTPL

Amounts in £‘000
Financial liabilities at FVTPL
Derivatives financial liabilities
Total liabilities at FVTPL

Year ended 31 December 2020
Level 3

Level 2

Level 1

–
–

1,834
1,834

–
–

Year ended 31 December 2019
Level 3

Level 2

Level 1

–
–

845
845

–
–

Year ended 31 December 2018
Level 3

Level 2

Level 1

–
–

5
5

1,415
1,415

Total

1,834
1,834

Total

845
845

Total

1,420
1,420

There were no transfers between Levels during the current or prior year.

The table above only shows the fair value of the financial liabilities as the fair value of the applicable financial assets are not materially 
different from their carrying value.

Fair value of financial liabilities that are not measured at fair value  
(but fair value disclosures are required)

Amounts in £‘000
Bonds
Convertible loan notes 
Short-term financing facilities

Amounts in £‘000
Bonds
Convertible loan notes 
Short-term financing facilities

Carrying amounts

Year ended 
31 December 
2020
–
–
–

Year ended 
31 December 
2019
4,108
2,248
721

Year ended 
31 December 
2018
953
3,750
79

Year ended 
31 December 
2020
–
–
–

Fair value
Year ended 
31 December 
2019
4,115
2,386
721

Year ended 
31 December 
2018
953
3,638
79

132

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47. AUDIT FEES

Fair value hierarchy of financial liabilities that are not measured at fair value (but fair value disclosures are required)

Bonds
Convertible loan notes
Bank loans at fixed interest rate
Accrued interest

Fair value 
hierarchy
3
3
3
3

There were no transfers between levels during the current or prior years.

45. COMMITMENTS GIVEN AND RECEIVED
As the Group has repaid all borrowings (excluding the lease liabilities) outstanding at December 2019, the related guarantees granted 
to the lenders no longer exist.

Amounts in £‘000
Fees payable to the Company’s Auditor and its associates in respect of the audit
Group audit of these financial statements
Audit of the Company’s subsidiaries’ financial statements
Total audit remuneration

Fees payable to the Company’s Auditor and its associates in respect of  
non-audit-related services
Audit-related assurance services
All other services
Total non-audit-related remuneration

Year ended 
31 December 
2020

Year ended 
31 December 
2019

144
 232
 376

–
14
14

84
95
179

 7
18
25

46. RELATED PARTIES
Parties related to Novacyt SA are:

•  the managers, whose compensation is disclosed below; and

•  the Directors of Novacyt SA.

Remuneration of key management personnel

Amounts in £‘000
Fixed compensation and company cars
Variable compensation
Social security contributions
Contributions to supplementary pension plans
Share-based payments – LTIP
Total remuneration

Aggregate directors’ remuneration

Amounts in £‘000
Fixed compensation and company cars
Variable compensation
Social security contributions
Contributions to supplementary pension plans
Fees
Share-based payments – LTIP
Total remuneration

Year ended 
31 December 
2020
867
495
899
40
14,233
16,534

Year ended 
31 December 
2019
990
113
140
47
–
1,290

Year ended 
31 December 
2020
705 
330 
658 
29 
33 
11,110 
12,866 

Year ended 
31 December 
2019
591
60
100
26
24
–
801

Related party transactions were made on terms equivalent to those that prevail in arm’s length transactions.

48. IMPACT OF BREXIT ON THE GROUP’S ACTIVITY
The UK left the EU on 31 January 2020, and the Brexit transition period ended on 31 December 2020 with a Trade and Cooperation 
Agreement (“TCA”) in place between the UK and EU. Our overriding priority in preparing for the UK’s exit from the EU has been to 
maintain continuity of supply of our products to customers. 

To date, the impact of Brexit has not had a material impact on the business but as we are in the early stages of the post-Brexit era, 
management continues to monitor and manage the situation.

49. SUBSEQUENT EVENTS 
After the year end, the Group received notification of a contract dispute (see note 50). 

50. CONTINGENT LIABILITIES
After the year end, the Group received notification of a contract dispute related to revenue totalling £129,124,000 in respect of 
performance obligations satisfied during the financial year to 31 December 2020. £23,957,000 of invoices in respect of products 
delivered during the year is outstanding at the date of signing the financial statements and recovery of the invoice is dependent on 
the outcome of the dispute. 

After the year end, a further £49,034,000 of product delivered and invoiced in 2021 is unpaid and part of the commercial discussions 
that are ongoing.

The Group has taken independent legal advice and a provision has been made in the financial statements in respect of 
management’s best estimate in respect of this claim (see note 30). 

Management and the Board of Directors have discussed the legal advice presented to them and have formed a judgment that, in 
accordance with the contractual terms, it should be possible to replace the products in dispute and a product warranty provision has 
been made accordingly.

If a claim under the limited assurance warranty is successful then management’s best estimate of the settlement cost is up to a 
maximum of £19,753,000, as per note 30, the timing of any outflow is dependent on settlement of the dispute. If no settlement is 
achieved and legal action is required, the timing of any possible outflow will be extended.

It is possible, but not probable, that the refund claim under the limited assurance warranty will be successful. The timing of any cash 
outflow is dependent upon the success of a claim and the terms negotiated for repayment. 

If the settlement of the claim is materially different from management’s determination of replacing the products, the financial 
statements with regards to revenue and the provision for product warranty could be significantly impacted.

134

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Glossary of terms

Company Information

Conformitè Europëenne 

coronavirus disease of 2019

clinical research organisation 

enzyme-linked immunosorbent assay

emergency use approval

emergency use listing

US food and drug administration

GlaxoSmithKline

in vitro diagnostic

lateral flow tests

long term agreement

polymerase chain reaction

point of care

quantitative polymerase chain reaction

ribonucleic acid

respiratory syncytial virus

research use only

United Nations Children’s Fund

variants of concern

CE mark

COVID-19

CROs

ELISA

EUA

EUL

FDA

GSK

IVD

LFT

LTA

PCR

POC

qPCR

RNA

RSV

RUO

UNICEF

VOC

136

Auditors 

Directors 

James Wakefield 
Graham Mullis 
Anthony Dyer 
Dr Andrew Heath 
Dr Edwin Snape 
Jean-Pierre Crinelli 
Juliet Thompson

Company Secretary 

Nick Plummer

Registered office 

Novacyt S.A. 
13 Avenue Morane Saulnier 
78140 Vélizy-Villacoublay 
France

Registered number 

491 062 527 (France)

Company website 

www.novacyt.com

Bankers 

(Nominated Advisor 
and Joint Broker) 

(Joint Broker) 

French Listing 
Sponsor 

Legal advisers to the 
Company 

S. P. Angel Corporate Finance LLP* 
Prince Frederick House
35-39 Maddox Street
London W1S 2PP 
United Kingdom

Numis Securities Limited
The London Stock Exchange Building
10 Paternoster Square
London EC4M 7LT 
United Kingdom

Allegra Finance 
213 Boulevard Saint-Germain 
75007 Paris 
France

English law:

Stephenson Harwood LLP 
1 Finsbury Circus 
London 
EC2M 7SH 
United Kingdom

Pitmans LLP 
47 Castle Street 
Reading 
RG1 7SR 
United Kingdom

French law:

Stance Avocats 
37-39 Avenue de Friedland 
Paris 75008 
France

Deloitte & Associés 
6 place de la Pyramide
92908 Paris-La Défense Cedex
France

Téléphone: +33 (0) 1 40 88 28 00
www.deloitte.fr
Adresse postale:
TSA 20303
92030 La Défense Cedex

Constantin Limited 
Statutory Auditor 
25 Hosier Lane 
London 
EC1A 9LQ 
United Kingdom

Banque Populaire Val de France 
Accueil Entreprises Trs 
2 Avenue De Milan 
37924 Tours Cedex 9

Barclays Bank plc 
48a - 50 Lord Street 
Liverpool 
L2 1TD 
United Kingdom

National Westminster Bank plc 
Southampton University 
Southampton Customer Service Centre 
Brunswick Gate 
23 Brunswick Place 
SO15 2AQ

Investec Bank PLC 
30 Gresham Street 
London 
3C2V 7QP 
United Kingdom

HSBC 
Bonham Strand Commercial Service 
Centre 
35-45 Bonham Strand 
Sheung Wan 
Hong Kong

Bank of China 
First Floor 
No. 50 Tai Nan Road 
Pudong 
Shanghai 
200131

Novacyt Group Annual Report and Accounts for the year ended 31 December 2020