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Keeping updated with GCP requirements

Sign up to:

  • MHRA Inspectorate Blog for an invaluable source of information on removal of drugs, drugs supplies, GCP/GLP symposiums and updates to regulatory and GCP practice
  • Health Research Authority (HRA) for all the latest news and developments

Check regularly:

  • MHRA GCP Forum
  • European Medicines Agency (EMA)
    • Q&A: Good Clinical Practice
    • GCP Inspectors Working Group
  • R&D Forum
  • Head of Agencies Clinical Trial Facilitation Group

Research and Development

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    • GCP Training
    • Keeping updated with GCP requirements
    • Protocol Guides for HEY-Sponsored CTIMPS and non-CTIMPS
    • GCP SOPs for HUTH-Sponsored CTIMPS
    • Non-CTIMPS
    • Research Passport: How to obtain an Honorary Contract or a Letter of Access with HEY Trust
    • Audit Tool
  • Performance in Initiating and Delivering (PID) Clinical Research
  • Daisy Appeal
  • Dementia Research
  • Contact R&D

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