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Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Guidance on 5 year housing land supply and Housing Delivery Test.
The information clients, principal designers, principal contractors and accountable persons need to keep.
How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Sets out the process for efficient and inclusive consultation of planning applications
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