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
Reports summarising work undertaken by the Minister for Equalities and government departments on COVID-19 disparities.
How to use chatbots and webchat tools to improve your users’ experience of your service.
Volume 29 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
You need to move to Universal Credit if you’ve received a Migration Notice letter, as one or more of your benefits will be ending soon.
The Trade Remedies Authority exists to defend the UK against unfair international trade practices. We investigate whether new trade remedies are needed to prevent injury to UK industries caused by unfair trading practices and make recommendations on appropriate measures to...
Provides guiding principles on how planning can deal with land affected by contamination.
Codes that DVLA places on your driving licence, and their explanations
Tell users how accessible your website or mobile app is in your accessibility statement, based on recent testing.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
The Independent Reviewer of Terrorism Legislation reviews the operation of the UK’s laws on terrorism, and writes up the findings and recommendations in regular reports. These reports are then laid before Parliament, to inform the public and political debate. Independent...
This series brings together all documents relating to TAB terms or reference
Information for health professionals and immunisation practitioners.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Exporters of groups of products of animal origin (POAO) to the EU and Northern Ireland can join the groupage export facilitation scheme (GEFS) to use 30-day support attestations.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
How to change the password, phone number or email address you use to sign in to your GOV.UK One Login.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
The Crown Commercial Service technology service principles help us to continually improve the way technology is bought across government and the public sector.
This note is part of the statutory guidance under s215 of the HRA 2008 (from 1 April 2024)
Guidance for the pharmaceutical industry on applying for a marketing authorisation for parallel import (MAPI).
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.