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Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to use a cost benefit analysis to evaluate your digital health product.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Use a separate statement of objection form for each Japanese GI product name you object to.
Check what you need to do to sell cosmetic products in Great Britain.
Information about the Working Group on Product Recalls and Safety.
Factsheets accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
Resources for individuals and organisations to use supporting a variety of safety awareness campaigns.
How to use an interrupted time series to evaluate your digital health product.
Information and resources.
How to use a cost utility analysis to evaluate your digital health product.
How to submit a cosmetic product notification to the Office for Product Safety and Standards (OPSS).
How to use a quasi-experimental study to evaluate your digital health product.
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How we will deliver protection and confidence in a strong, green economy.
Guidance on choosing evaluation study types and methods.
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