How will clinical trials be regulated after 1 January 2021?
At the end of the Brexit transition period the UK are working towards maintaining a robust process in clinical trials regulation. UK Clinical Trial Applications (CTAs) will continue to be authorised by the Medicines and Healthcare product Regulatory Agency (MHRA) and UK Ethics Committee (EC). Thus, the UK’s ability to participate in multinational trials will not change. Existing clinical trial approvals in the UK will continue to apply and there will be no requirement to re-apply.
Download our recent whitepaper so that after reading you will have an answer to the question 'How will clinical trials be regulated after 1 January 2021?'.