Patient and family experiences inform antidepressant safety information review

Clinical trial applications that need expert advice from a specialist group or committee.

A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.

Professor Anthony Harnden has congratulated the trio of Agency board members on the extension of their appointments.

List of Field Safety Notices from 1 to 5 September 2025.

Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.

Information on the new regulations for the post-market surveillance of medical devices which come into effect on 16 June 2025.