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Register to vote Register by 18 June to vote in the General Election on 4 July.
Submission dates and how the submissions using the EC decision reliance procedure work.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
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…
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
How the MHRA processes variations to Marketing Authorisations (MAs)
Find out if you will need to use the new UKNI marking and how to use it.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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.
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 on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
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.
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