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Guidance to assist fishers understand the role of I-VMS and their responsibilities.
Learn how the Government Digital Service is monitoring accessibility under the Public Sector Bodies (Websites and Mobile Applications) (No.2) Accessibility Regulations 2018.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Official information British people moving to and living in the United States of America (USA) need to know, including residency, healthcare and driving.
The Planning Inspectorate appeals casework portal - Terms and Conditions
Learn how to check if your website or mobile app is accessible.
Find out about group and divisional VAT registration and the forms you should use to apply.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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