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A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without an authorisation.
Find out how to submit brand details to HMRC for Scotch Whisky, Irish Whiskey, Irish Cream, Irish Poteen, Somerset Cider Brandy and Single Malt Welsh Whisky if you're a verified bottler.
UK government interpretation of the requirements for labelling e-liquids for Great Britain
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Requirements for importers, retailers and wholesalers selling and labelling wine in Great Britain, including labelling laws for wine imports into England from 1 January 2024.
This guidance provides an introductory guide to the standards and regulatory requirements that businesses may need to meet, to import and sell goods in the UK.
You must batch and label the beef and veal you sell or supply according to specific rules, which vary from product to product.
Supporting documents containing information about the use and labelling of food supplements in England.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Check what you need to do to sell cosmetic products in Great Britain.
How to conform with the legal requirements for placing medical devices on the market.
This guidance explains the legal framework for labelling and packaging as described in UK legislation and gives best practice for producing medicines labelling and packaging.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
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