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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
The way you apply to licence biological products has changed
Find out when you can zero rate books and other forms of printed matter.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
Fake, potentially harmful Ozempic and Saxenda pens have been found in the UK: you should only access these medicines via a medical prescription.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
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.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
When charities can trade, tax rules and when to trade through a separate company.
How to renew marketing authorisations for products granted through different routes and at different times.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Marketing standards for hops producers, manufacturers, retailers and distributors.
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