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How to complete and submit the turnover declaration form as the holder of a UK marketing authorisation.
Form for listing all weapons and their serial numbers in the possession of a private maritime security company (PMSC).
Apply for a public health exemption from the sunset clause.
How to renew marketing authorisations for products granted through different routes and at different times.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.…
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
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 package medicines for sale and what information you must provide to consumers and healthcare professionals.
What private maritime security companies (PMSCs) need to provide to comply with licence conditions.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Use this form to request approval for new third parties to be added to your open general trade control maritime anti-piracy licence (OGTCL MA-P) approval letter.
Find the difficulty level of a qualification and compare qualifications across different countries.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
How to transport dangerous goods, including guidance notes, authorisation notices, exception notices and multilateral agreements.
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