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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.
Guidance for the veterinary pharmaceutical industry on how to apply for and maintain a joint-label for use on veterinary medicines placed on the market in the UK and Ireland.
You must batch and label the beef and veal you sell or supply according to specific rules, which vary from product to product.
Rules about the labels that tyres must display to give information about fuel efficiency, wet grip and noise classification.
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.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Find out when you must label your meat, fish or seafood product with its country of origin.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
Guidance for suppliers and dealers.
Music industry voluntary code that is a commitment to standards of good practice in relation to music streaming.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
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