We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
The MHRA has today set out its strategic approach to artificial intelligence (AI)
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.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
How to renew marketing authorisations for products granted through different routes and at different times.
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 to request and manage school-led initial teacher training (ITT) places for School Direct.
How to market, trial and release GMOs.
Guidance for manufacturers, importers and distributors.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Submissions related to human medicines need to be submitted directly to the MHRA.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.