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If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Things to consider when buying and using products.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Guidance on the many ways for suppliers to work with the Defence Science and Technology Laboratory (Dstl), the science inside UK defence and security.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Find out what a composite product is, and how to import or move composite products from the EU to Great Britain.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
How to import or move animal by-products from the EU to Great Britain.
Exporters of groups of products of animal origin (POAO) to the EU and Northern Ireland can join the groupage export facilitation scheme (GEFS) to use 30-day support attestations.
How to object to an application to use or change a traditional term for a wine product on the UK traditional terms register.
How to import or move food and drink from the EU to Great Britain.
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