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Find out about the registered dealers in controlled oil (RDCO) scheme.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Find out about the different simplified declarations for imports and what you need to do to get authorisation to use them.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Guidance for suppliers and dealers.
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.
Waste electrical and electronic equipment (WEEE) - retailer and wholesaler responsibilities, waste collection and compliance schemes.
Manufacturer licences including importer licences, specials, investigational and non orthodox and wholesale distribution licences.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Requirements for excise goods held in duty suspension in a warehouse by an authorised warehousekeeper, registered owner, duty representative or registered consignor in the UK.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Supplier declarations are where your UK supplier provides you with information needed to prove the origin of your goods for preferential rates of duty between the UK and other countries.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
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