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More information2nd April 2026
Summary:
The UK has published updated guidance on complying with ICH E6 Good Clinical Practice (GCP), setting out the standards expected for the design, conduct, recording and reporting of clinical trials involving medicines. The guidance clarifies responsibilities for sponsors, investigators and trial teams, and aligns UK expectations with international best practice while reflecting the UK regulatory framework. It aims to ensure participant safety, data integrity and ethical conduct across all stages of a clinical trial, supporting high-quality research and regulatory compliance.