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Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Standardisation explained.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
Legal standards for labelling and composition of food products such as bottled water, milk and meat.
Animal by-products (ABPs) you can use to make pet food, how to provide samples, and how to package your products.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Submission dates and how the submissions using the EC decision reliance procedure work.
When a material is waste, is a by-product or meets ‘end of waste’ status.
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
Check what you need to do to sell cosmetic products in Great Britain.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Information and guidance on a range of medical devices for users and patients.
Quality reports pull together key information showing how the various dimensions of quality have been considered.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Guidance for manufacturers, importers and distributors.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
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