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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Use data more effectively by improving your technology, infrastructure and processes.
This guidance covers how to run your API as a service, including building the team you will need and the lifecycle of your API
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Optimise your API service level indicators based on your user needs.
The team capabilities available on the Digital Outcomes framework.
Rules which govern the operation of the Forensic Information Databases strategy board.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
If you already have the right or have probate (as an executor or administrator) you can start dealing with the estate. You may need to apply for the right to deal with the estate of the person who's died (also...
We review decisions made by people or bodies with a public law function, eg local authorities and regulatory bodies. We can: carry out a judicial review of decisions made by other courts, tribunals and public bodies hear challenges to decisions...
Why to deploy regularly, deployment principles to follow, and how to do it.
This guidance is an introduction to the Open Document Format (ODF) standard and how you can select ODF-compliant solutions.
Resources, tools and guidance to help you manage and share your geospatial data and/or data in a FAIR (Findable, Accessible, Interoperable and Reusable) way.
How to create an MyHMCTS organisation account to manage, submit and pay for certain civil, family and tribunal cases.
The National DNA Database Ethics Group provides independent advice on ethical issues surrounding the operations of the database to Home Office ministers and the National DNA Database Strategy Board.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How you can test and manage your API when it is in alpha development.
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
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