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How to use a cost utility analysis to evaluate your digital health product.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How a marketing authorisation holder should report a defect with a veterinary medicine.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How the Office for Product Safety and Standards contributes to the national regulatory landscape.
Check what you need to do to sell cosmetic products in Great Britain.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Guidance for manufacturers and importers.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Product recall for eleven models of life jackets sold via Amazon presenting a serious risk of drowning.
How to use a behaviour change techniques review to evaluate your digital health product.
Guidance for manufacturers, importers and distributors.
Things to consider when buying and using products.
What you need to know about and do to comply with the law and keep consumers safe.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
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