Plans for Clinical Trials Post Brexit

Date: 01 November 2019

Plans for clinical trials in the event of a no-deal Brexit have been published by both the Health Research Authority and the Medicines and Healthcare products Regulatory Authority. 

This advice includes: changes to sponsors/legal representatives, IMP certification and importation, amendments to the Research Ethics Committee, and transferring research data between countries.

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  • Summary:
    The HRA and MHRA have published plans for clinical trials in the event of a no-deal Brexit.