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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…
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How the MHRA processes variations to Marketing Authorisations (MAs)
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
How to renew marketing authorisations for products granted through different routes and at different times.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
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