Stuart Haiz
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This blog shares the work of the Medicines and Healthcare products Regulatory Agency (MHRA) Inspectorate, by inspectors and those the Inspectorate works with.
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- Public Consultation on the International Council for Harmonisation ICH E6 (R3) Guideline for Good Clinical Practice Annex-2
- DSUR Submissions and Fees are Changing from 1 June 2024
- Pharmacovigilance unravelled: highlights of the 2024 MHRA GPvP Symposium
- Pilot GMP Single Inspection Program
- MHRA Pharmacovigilance Symposium 2024