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Submission dates and how the submissions using the EC decision reliance procedure work.

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.

How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.

Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.

A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.

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.

What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.

What to do if you think you've spotted a scam pretending to be from Companies House, and examples of scam emails, letters and telephone calls.

Find a BFPO number, send mail to and from British forces personnel and their families

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