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Register to vote Register by 18 June to vote in the General Election on 4 July.
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.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Submission dates and how the submissions using the EC decision reliance procedure work.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Find out how to account for VAT schemes on business gifts, samples and promotional schemes.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How the MHRA processes variations to Marketing Authorisations (MAs)
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Guidance for manufacturers, importers and distributors.
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.
How to use an interrupted time series to evaluate your digital health product.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to renew marketing authorisations for products granted through different routes and at different times.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
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