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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How property professionals can add, remove and amend transferor details – and their attorneys – in applications submitted through the Digital Registration Service.
When you can share information about your case, what you can share and what to do if someone else shares information.
A guide to documenting how you’ve collected your packaging data, known as your ‘methodology’. Online marketplaces affected by extended producer responsibility (EPR) for packaging must submit a methodology. This is also recommended for all producers as part of their ways...
Practical steps to manage the risk of online harms if your online platform makes users’ account details and activity visible to others.
How responders can reduce the risk of communications disruption during emergencies by using ResilienceDirect, HITS and Telecoms Sub-Groups.
Solicitors and barristers: how to submit any changes in your details to the Legal Aid Agency.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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.
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