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This guidance about notifying other landowners applies to planning, householder, minor commercial and listed building consent appeals.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
The information clients, principal designers, principal contractors and accountable persons need to keep.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Since, April 2024, the MHRA has been using Lorenz DocuBridge for eCTD management in product licence submissions. This change is part of the modernisation of the MHRA’s Legacy Systems and is one of the initial tools launched in the RegulatoryConnect...
A suite of template legal documents to support the development of mutuals.
How to change the ownership from one marketing authorisation (MA) holder to another.
This policy explains how accessible the documents the Independent Prevent Commissioner (OIPC) publishes on GOV.UK are.
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