Clinical trials for medicines: roles and responsibilities

16th April 2026

Summary:
This guidance sets out the key roles and responsibilities involved in conducting clinical trials for medicines in the UK, helping sponsors, investigators and other stakeholders understand their obligations. It explains how responsibilities are shared across those designing, managing and delivering trials, including ensuring participant safety, maintaining data integrity and complying with regulatory requirements. The document also highlights the importance of clear oversight, proper delegation and adherence to Good Clinical Practice to support high-quality and ethical research. Link: https://www.gov.uk/government/publications/clinical-trials-for-medicines-roles-and-responsibilities/clinical-trials-for-medicines-roles-and-responsibilities

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