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VICH consultation on the guideline relating to good manufacturing practice for active pharmaceutical ingredients used in veterinary medicinal products.
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Advice on ingredients in nicotine-containing liquids in electronic cigarettes and refill containers.
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Requirements for Immunological Veterinary Medicinal Products.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
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.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Requirements for Biological Veterinary Medicinal Products other than Immunological Veterinary Medicinal Products.
Find out the information you must give to customers on food products and how to give it.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Explainer for businesses and persons regulated by the Veterinary Medicines Regulations 2013, as amended, on the transitional provisions included in the amending legislation: the Veterinary Medicines (Amendment etc.) Regulations 2024.
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