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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…
This page provides information on branding and publicity for the UK Shared Prosperity Fund.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
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 who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
How the MHRA processes variations to Marketing Authorisations (MAs)
Rules on using a geographical indication (GI) scheme logo to mark a registered protected food or drink name.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How to renew your patents, trade marks or registered designs: when to renew, how to renew online or renew and restore by post, how much it costs.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Register a design - what designs are protected, search the registers, prepare your illustrations, how to apply, disclaimers and limitations.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to use an interrupted time series to evaluate your digital health product.
Cancel a marketing authorisation, traditional herbal registration or parallel import product licence or withdraw a pending submission.
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