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How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Resources to help anyone developing or running a digital health product to conduct an evaluation.
This page lists all the Regulatory Policy Committee's opinions.
This guidance provides an overview of the different tariffs for products exported to the UK under the DCTS, including how to identify commodity codes.
How to use focus groups to evaluate your digital health product.
A series of reviews by Ofsted looking at the research evidence currently available about different curriculum subjects.
Our Assurance products and guidance has been updated. Related guidance and tools are being refreshed and future revised versions will be published on an iterative basis. To ensure you are using the latest versions, you are advised to regularly access...
Guidance for manufacturers, importers and distributors.
Knowledge and Library Services (KLS) can provide support to conduct systematic reviews.
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