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This series brings together all documents relating to Guidance and methods
Guidance on various aspects of the planning system, given in letters to chief planning officers of local planning authorities.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This page collates the various existing ethical principles for data and AI, developed by government and public sector sector bodies. It intends to provide clarity and guidance for public servants working with data and/or AI.
Standards and standardisation explained.
Guidance on degree awarding powers, university title, designation for HEFCE funding and further education to higher education transfers.
Provides an introduction to National Infrastructure Planning Guidance.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This guide aims to improve the way functional work is done across government, by making it easier for people to comply with functional standards.
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