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Life Sciences

 
HMRC R&D Tax Credit Statistics for 2023-24
2,565 Claims
£1.15 Billion Claimed in this Industry
£428,850 Average Claim Size
HMRC Band C21 & 72 - Manufacture of basic pharmaceutical products and pharmaceutical preparations. Scientific research and development.
INTRODUCTION

Understanding R&D within the Life Sciences Sector

Accessing R&D tax relief in the UK requires more than identifying innovation at a surface level. It relies on translating complex scientific and technical activity into a structured, compliant narrative that aligns with HMRC expectations. Businesses operating in highly specialised fields benefit from working with advisors who understand both the regulatory landscape and the realities of delivering cutting-edge work. With the right approach, companies can ensure their R&D activity is accurately captured, robustly supported, and positioned to withstand scrutiny, while maximising the value of the relief available.

 

There is a well-established connection between R&D tax relief and the life sciences sector, although the boundaries of what qualifies are often misunderstood. Most day-to-day activity will not meet the criteria, and claims are rarely all or nothing. The focus should not be on commercial outcomes, but on identifying genuine advancements in science or technology relative to existing knowledge, and whether achieving them required resolving uncertainty that a competent professional could not easily overcome.

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Core Sectors Within Life Sciences

The six main industry areas that make up the life sciences sector
Pharmaceuticals Develop, manufacture, and commercialise medicines, including small-molecule drugs and advanced therapies, to prevent, manage, or cure disease  
Biotechnology Develop technologies based on cell therapy, gene therapy and biologics to treat life-threatening diseases.  
Medtech Design and produce devices, instruments, implants, and hardware used to diagnose, monitor, or treat patients.  
Diagnostics and testing Create tests, assays, and lab platforms that detect disease, measure biomarkers, and support clinical decision-making.  
CRO/CDMO services Provide outsourced research, development, clinical trial, manufacturing, and formulation services for life sciences companies.  
Healthtech Build software, data, and AI-enabled tools that improve care delivery, patient monitoring, treatment access, and health outcomes.  

Examples of R&D activity in Life Sciences:

  • Drug Discovery and Molecular Research:
    Applying pharmacological knowledge to predict or discover new drug candidates, including routine methods like high-throughput screening, where the activity advances scientific knowledge.
  • Preclinical & Clinical Development:
    Laboratory testing and clinical trials (phases I–III), including payments to participants, form a core R&D activity.

  • Medical Devices:
    Developing new devices with unknown performance or safety profiles, such as drug-eluting stents, involves significant R&D in manufacturing ultra-thin structures and ensuring controlled delivery mechanisms.

  • Formulation & Drug Delivery:
    Creating new drugs or delivery methods, such as fridge-free vaccines, involves solving complex scientific challenges around stability, efficacy, and manufacturability.
  • Formulation & Drug Delivery:
    Creating new drugs or delivery methods, such as fridge-free vaccines, involves solving complex scientific challenges around stability, efficacy, and manufacturability.

  • Diagnostic Tools:
    Developing novel tools or processes, including AI-driven diagnostic imaging, enables earlier diagnosis and improves patient outcomes.

  • Biotechnology:
    Innovations in gene therapies and personalised medicine, including inserting genes in vivo, push the frontier of biological knowledge.


This is not an exhaustive or definitive list. It should be considered a starting point only. Every project must be evaluated individually based on its unique technical challenges and merits.

What Does This Relief Translate to in Real Terms?

To help bring this into context, we've included a selection of anonymised client examples showing the types of projects that have qualified, along with the level of relief they were able to claim.

What doesn’t count as R&D in the life sciences sector?

  • Packaging changes to pharmaceutical/biotech products
  • Using off-the-shelf laboratory equipment and reagents as intended
  • Standard regulatory compliance and routine documentation
  • Developing existing drugs, diagnostics, or medical devices
  • Standard regulatory compliance and routine documentation
  • Post-market surveillance and routine pharmacovigilance
INSIGHTS PREVIEW

WHAT WE HAVE TO SAY

Our fantastic team of report writers have prepared articles covering the land of tax extensively. If you have a question relating to accounting or tax, it's likely we've already written the answer.

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The Claim Process

We understand the complications that can often arise when completing an R&D claim, not to mention the significant amount of time it can consume, diverting your attention from driving your innovation forward. That's why we have streamlined a transparent and hassle-free process that follows a step-by-step approach from start to finish.

Throughout your R&D claim process, we maintain open lines of communication tailored to your preferences. Once we have compiled comprehensive technical and financial reports, we take the responsibility of submitting them and proactively follow up with HMRC, leading the communication on your behalf. Often, our next contact with you brings the exhilarating news of success and positive outcomes.

  • Step 1

    We'll gain your authorisation via our client instruction form/NDA. This will enable us to discuss your R&D activities along with your current tax position. This will enable us to discuss your R&D activities along with your current tax position.
  • Step 2

    We'll analyse the profit & loss (P&L) statement of the business while facilitating your technical call. This step aims to determine whether your case is feasible from both technical and financial perspectives.
  • Step 3

    Once our experts are confident that your case meets the R&D eligibility criteria, we will then gather all the required technical information and financial documentation according to HMRC's standards to support your case.
  • Step 4

    At this stage, we initiate a stringent compliance procedure that we have developed in-house to audit your R&D claim application. We verify whether it meets the defined standards before submitting it to HMRC to ensure a positive outcome.
  • Step 5

    After conducting a comprehensive review of your R&D claim, including all required documentation, the application will be forwarded to HMRC for further processing.
  • Step 6

    Our team maintains continuous contact with HMRC regarding your case. If any queries arise, we address them on your behalf using a highly systematic approach to maximise your outcome while minimising any delays in your repayment.
HOW EFFECTIVE ARE

DSIT Guidelines

The DSIT Guidelines form the foundation for compliance when preparing an R&D claim. In conjunction with the wider scope of HMRC’s guidance in relation to R&D Tax Relief, they set out how to determine whether work qualifies and provide practical examples of how to apply the criteria to evidence R&D within a project. These guidelines should not only underpin the assessment process when compiling a claim but can also be referenced during an enquiry defence if required. By demonstrating to HMRC how a project aligns with the definitions and scenarios outlined, you can clearly evidence that the innovation undertaken qualifies for R&D tax relief. Below are five of the guidelines we most frequently rely on to support qualifying work. 

DSIT 3 Software projects aim to advance knowledge or capabilities within the sector, often addressing challenges in system architecture, platform integration, or scalable software design.  
DSIT 7 Companies often seek to advance a field of science or technology which can have either tangible consequences, such as improving the security of a system by implementing a segmented software architecture for an existing system; or intangible consequences, such as new knowledge regarding integrations of legacy products or the behaviour of various data structures.   
DSIT 9 A project may extend overall knowledge, create a process or device, make an appreciable improvement to an existing process, or duplicate the effect of an existing product, to name a few types of qualifying activity.  
DSIT 11 If a particular advance in software engineering has already been made or attempted but details are not readily available, work to achieve such an advance is R&D. For example, where a software company has already developed a process that could more accurately consolidate disparate data sets, but the process is a trade secret, a company seeking to develop a similar process is still considered R&D.  
DSIT 21 Overall knowledge or capability can still be advanced in situations where companies are working in the same field independently, work is a trade secret, or where the details are not readily available; even where it is known that a particular advance has already been achieved.   

HMRC often reference software development examples throughout its guidance.

Drawing direct comparisons to HMRC’s own examples offers a clear and simple way to evidence compliance in R&D projects, whether relating to a single technical detail or an entire scheme. 

The following pages set out examples drawn directly from HMRC’s published guidance, which we reference where relevant within our reports. 
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A company is conducting R&D in the development of a software service for the commercial banking market in the US. Development requires the company to have a collocated team in the US due to access regulations within the US banking sector. This requires conditions (the presence of US banking systems and regulatory requirements) which are not present in the UK, and which would be wholly unreasonable to replicate. 

This condition exists in the US. Therefore, this activity would satisfy CTA09/1138A if undertaken in the US, where the necessary conditions arise. Under the new ‘merged’ R&D scheme, overseas costs that used to be claimable may be blocked from a claim and so it’s important to ensure your work remains compliant in the modern R&D landscape.

CIRD152000, Example 5

In determining the relevance of your R&D work, we firstly assess whether the work advances your field of science of technology, however we then need to consider what makes your work technologically or scientifically uncertain. A technological or scientific uncertainty exists when knowledge of whether something is scientifically possible or technologically feasible, or how to achieve it in practice, is not readily deducible or available by a competent professional working in the field as per S.13 DSIT guidelines.

CIRD81960

Managing Enquiries - Case Studies?

The following examples illustrate how investing in R&D can deliver tangible results, especially in complex software projects. They are presented from a tax perspective rather than a technical viewpoint, explaining projects in a way that HMRC will recognise and accept, rather than using traditional industry language. Each study focuses on how the project is described, rather than providing a full breakdown of the DSIT guidelines applied. For further detail, more comprehensive case studies are available on the Wilby Jones website.

CONCLUSION

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Explore additional solutions for your Life Science project

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