Medicines: get scientific advice from the MHRA
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A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
Adapted edition
- Document type
- Reference Guide
- Format
- DOCX
- Pages
- 7
- Language
- English
- Version
- 1.0
- Updated
- 2026-09-17
- Category
- Safety & operations
- Licence
- Open Government Licence v3.0
Description
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved. Consult the original guidance for current legal and operational details.
Contents
- Overview
- Process and timelines
- MHRA expertise on offer
- Types of meeting
- Scientific advice meeting
- Broader scope advice meeting
- Joint scientific advice with the MHRA and NICE
- Real-World Data (RWD) and Real-World Evidence (RWE) advice
- Devices, in vitro diagnostic devices and Clinical Investigations regulatory advice meetings
- Regulatory advice
- Ask for scientific advice
- After the form is completed
- Supporting document guidance
- Briefing document(s)
- Questions you need advice on
- Before the meeting
Source and licence
Medicines and Healthcare products Regulatory Agency
AttributionMedicines and Healthcare products Regulatory Agency, ‘Medicines: get scientific advice from the MHRA’ (updated 14 August 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