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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
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.
Special feature articles on energy issues in the United Kingdom from the quarterly statistical bulletin Energy Trends.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
FCDO travel advice for Ecuador. Includes safety and security, insurance, entry requirements and legal differences.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The review of the safety of isotretinoin has concluded.
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