Updated guidance is now available to assist trial sponsors in building resilience into new and ongoing trials during the continuing pandemic.
Manager, Clinical Trials Unit
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About the MHRA Inspectorate Blog
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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- Pharmacovigilance inspection metrics April 2019 to March 2020
- Guidance on pharmacovigilance requirements for UK authorised products from 1 January 2021
- Reference Safety Information (RSI) for Clinical Trials- Part III
- Pharmacovigilance requirements for UK authorised products - 13 January 2021
- Post-transition: Pharmacovigilance requirements for UK authorised products - Thursday 22 October 2020