Clinical trials for medicines: expert advice
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Clinical trial applications that need expert advice from a specialist group or committee.
Adapted edition
- Document type
- Reference Guide
- Format
- DOCX
- Pages
- 4
- Language
- English
- Version
- 1.0
- Updated
- 2026-09-17
- Category
- Safety & operations
- Licence
- Open Government Licence v3.0
Description
Clinical trial applications that need expert advice from a specialist group or committee. Consult the original guidance for current legal and operational details.
Contents
- Legal status of this guidance
- Trials requiring expert advice
- Where the applicant identifies the need for expert advice
- Where the authorities identify the need for expert advice
Source and licence
Medicines and Healthcare products Regulatory Agency
AttributionMedicines and Healthcare products Regulatory Agency, ‘Clinical trials for medicines: expert advice’ (updated 28 April 2026), reused under the Open Government Licence v3.0.
ChangesNeutral text-only adaptation from the official GOV.UK Content API body: headings, paragraphs, ordered and unordered list items and clickable source-link destinations in an appendix preserved. Images, logos, page design, accessible-format request widgets and linked attachments excluded; normalised whitespace, invisible format marks and typography.
Version history
- v1.017/09/2026