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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Use our voluntary advance checks form to pre-submit details of EU firearms dealers to Export Control Joint Unit (ECJU).
Templates for members of the Distributor Take-back Scheme (DTS) under the waste electrical and electronic equipment (WEEE) regulations.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Information about the EU Regulations and their implementation in Northern Ireland
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
You must get permission to export certain drugs and medicines.
List of sites granted a manufacturer or wholesale dealer licence
Licence and registration application information for companies that deal in precursor chemicals.
Advice on writing clear notices and maximising replies to your FSNs.
Guidance for manufacturers, importers and distributors (including retailers).
Find out how to declare that your goods have been put to their authorised use, destroyed or re-exported.
Use the online service HO4 to apply to be approved as a registered dealer in controlled oil.
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