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Contents

Official guidance
Corporate Intangibles Research and Development Manual

CIRD130000 · R&D tax reliefs: reformed reliefs: categories of qualifying expenditure

  • CIRD131000 · Overview
  • CIRD132000 · Payment condition
  • CIRD133000 · Staffing costs
  • CIRD133100 · Staffing costs: measure of staffing costs
  • CIRD134000 · Software
  • CIRD135000 · Data licenses and cloud computing services
  • CIRD136000 · Software, data licenses, cloud computing services and consumables: consumable items
  • CIRD136100 · Software, data licenses, cloud computing services and consumables: consumable items: meaning of consumed or transformed
  • CIRD137000 · Externally provided workers
  • CIRD137100 · Externally provided workers: definition
  • CIRD138000 · Contractor payments
  • CIRD139000 · Relevant payments to the subjects of a clinical trial
  1. R&D tax reliefs: reformed reliefs: categories of qualifying expenditure: contents
  2. R&D Tax Reliefs: reformed reliefs: categories of qualifying expenditure: relevant payments to the subjects of a clinical trial

CIRD139000 | R&D Tax Reliefs: reformed reliefs: categories of qualifying expenditure: relevant payments to the subjects of a clinical trial

From HM Revenue & Customs · Corporate Intangibles Research and Development Manual

Clinical trial participants in the pharmaceutical industry

When pharmaceutical companies develop a drug they have to gain the approval of regulatory authorities in order to market the drug. The process of approval involves the appraisal of the safety and efficacy of the drug in a series of clinical trials. These are described at CIRD81920.

The trials involve the testing of the drug in both healthy patients and patients with the target disease or condition. Pharmaceutical companies and contract research organisations will often make payments to people taking part in clinical trials. Trials are conducted under ethical guidelines and the nature of the trials and what is expected of the participants will be fully explained to them and documented.

The cost of relevant payments to subjects of clinical trials can be claimed for under both new RDEC and ERIS. A ‘relevant payment’ is defined as a payment made to the subject of the trial in return for participating in the trial. The term ‘clinical trial’ is defined as ‘an investigation in human subjects undertaken in connection with the development of a health care treatment or procedure’ (CTA09/S1140).

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