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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.
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.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
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.
The review of the safety of isotretinoin has concluded.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Learn about about importing and exporting goods.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
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