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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
When you can share information about your case, what you can share and what to do if someone else shares information.
Practical steps to manage the risk of online harms if your online platform makes users’ account details and activity visible to others.
Solicitors and barristers: how to submit any changes in your details to the Legal Aid Agency.
How responders can reduce the risk of communications disruption during emergencies by using ResilienceDirect, HITS and Telecoms Sub-Groups.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
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