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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
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Blogs where government organisations talk about their work and share information and ideas.
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.
Marketing authorisations (MAs) granted since January 2014.
Use this form to notify the IPO of marketing authorisation for a medicinal or plant protection product, granted after your application for an SPC for that product.
Guidance to renew your marketing authorisation including the renewal form.
VisitBritain (VB) is the national tourism agency, responsible for marketing Britain worldwide and developing Britain’s visitor economy. It works with UK Trade & Investment as well as airlines, travel operators, global brands and the official tourism bodies for London, England,...
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.
How sellers deal with VAT for goods from overseas that they sell direct to customers in the UK.
The way you apply to licence biological products has changed
The official UK government website for data and insights on COVID-19.
Marketing authorisations granted in 2024
This series brings together all documents relating to DECC exceptions to moratoria on spend for ICT, consultancy, recruitment, property, consultancy, advertising and marketing.
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