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If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
All marketing and advertising must be: an accurate description of the…
Advertising to consumers The Consumer Protection from Unfair Trading…
There are 2 advertising codes of practice that describe how businesses…
You must describe your product accurately. This means if you make a claim…
You must check if customers want to be contacted by fax, phone, post or…
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
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.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How the MHRA processes variations to Marketing Authorisations (MAs)
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.
UKHSA Chief Executive Professor Dame Jenny Harries visits Manchester and Liverpool to launch campaign as measles cases continue to rise.
Guidance on the European Union regulation on explosives precursors, including licensing, labelling and reporting suspicious activity
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Declaration for approval under Commission Regulation 1019/2002.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
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