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Register to vote Register by 18 June to vote in the General Election on 4 July.
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,...
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
The CMA is investigating whether Google might have abused a dominant position through its conduct in ad tech
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Cancel a marketing authorisation, traditional herbal registration or parallel import product licence or withdraw a pending submission.
COI was the government department responsible for providing marketing and advertising services to other organisations in the public sector. COI closed in 2012.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Find out about the off-payroll working rules (IR35) for agencies, when the changes to these rules apply and how the changes will affect you.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
The VOA has standards of behaviour we expect of agents.
FCDO travel advice for Germany. Includes safety and security, insurance, entry requirements and legal differences.
ARIA will focus on projects with potential to produce transformative technological change, or a paradigm shift in an area of science. ARIA is an executive non-departmental public body, sponsored by the Department for Science, Innovation and Technology .
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
Don’t include personal or financial information like your National Insurance number or credit card details.
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