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Simplifying the process of seeking and recording consent in low risk clinical trials

 

The Health Research Authority is proposing changes to the UK’s Clinical Trials regulations to simplify the way that informed consent is sought and recorded in low risk clinical trials.

They want to ensure that the proposed changes work for everyone, using an approach that people can trust.

The HRA is asking for feedback on their proposed changes to the current process, and are asking for the research community and members of the public to complete a short survey.

All of the feedback you share will be used to shape the new Clinical Trials regulations in the UK and the accompanying guidance that the HRA is producing.

The survey closes on Friday 10 January 2025.

If you have any questions about the survey please email: communications@hra.nhs.uk

Find out more and complete the survey