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Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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 a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
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