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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.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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.
Submissions related to human medicines need to be submitted directly 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.
Submission dates and how the submissions using the EC decision reliance procedure work.
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
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