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Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Criteria applied by the VMD for accepting and agreeing the invented name of veterinary medicinal products.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
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