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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Advice on how to stay secure online from the UK's National Cyber Security Centre.
Submissions related to human medicines need to be submitted directly to the MHRA.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Find out how to import your personal belongings, pets and private motor vehicles when moving or returning to the UK.
How investigators and sponsors should manage clinical trials during COVID-19
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
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