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Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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The official UK government website for data and insights on COVID-19.
How to conform with the legal requirements for placing medical devices on the market.
The Export Control Joint Unit (ECJU) administers the UK’s system of export controls and licensing for military and dual-use items. ECJU is part of the Department for Business and Trade .
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
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Details of General Licences issued by OFSI
List of fees for consular information in the USA.
Find registered patents, patent applications and pending patents
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Get information on teacher training courses, funding, pay scales and how to make a great application
List of Field Safety Notices from 22 to 26 April 2024.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Information about the EU Regulations and their implementation in Northern Ireland
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
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