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Employment Appeal Tribunal Judgment of Mrs Justice Eady on 3 May 2024.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Apply for a higher education course, track your application and accept or reject your offers.
Find registered patents, patent applications and pending patents
List of fees for consular information in the USA.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
This page provides practical information to help you make the most of your IP when doing business in Kazakhstan.
You may need a visa to come to the UK to visit, study or work.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
Check how much your visa application costs in the country you’re in
Use this form to file a translation in connection with a European patent or a European patent application
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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