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Join a Health Research Authority (HRA) advisory group on informed consent in certain clinical trials

Clinical trials aim to find out more about an illness, condition, treatment, therapy or care. The type of clinical trials we are discussing in this work involve medicines routinely used in the NHS which have therefore undergone all necessary safety evaluations required for use in the UK.
We are developing principles on simplified arrangements for consent to support these important clinical trials on existing medicines, while maintaining public trust.