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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…
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
The seeds which must be certified before you can market them, how to get them certified and how to get a licence for your seed business.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Submissions related to human medicines need to be submitted directly to the MHRA.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Marketing standards for veal and beef importers, exporters, producers, manufacturers, retailers and distributors.
How the MHRA processes variations to Marketing Authorisations (MAs)
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information about new applications, post-licensing, advertising, product information and fees.
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.
Pharmacovigilance system requirements
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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