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Register to vote Register by 18 June to vote in the General Election on 4 July.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How to use an interrupted time series to evaluate your digital health product.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
How to create a model of how your digital health product works and choose measures for your evaluation.
How to use a quasi-experimental study to evaluate your digital health product.
Use these general provisions to help you determine the origin of your products.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How we are building national capacity for product safety.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Check what you need to do to sell cosmetic products in Great Britain.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How to use a before-and-after study to evaluate your digital health product.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Guidance on choosing evaluation study types and methods.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
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