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Register to vote Register by 18 June to vote in the General Election on 4 July.
Employment Appeal Tribunal Judgment of Sarah Crowther, Deputy Judge of the High Court on 24 May 2024.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Upper Tribunal Administrative Appeals Chamber decision by Judge Citron on 18 April 2024.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
Upper Tribunal Administrative Appeals Chamber decision by Judge Citron on 3 May 2024.
What businesses need to do to import ‘relevant’ nuclear materials into the UK.
How responders can reduce the risk of communications disruption during emergencies by using ResilienceDirect, HITS and Telecoms Sub-Groups.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Upper Tribunal Administrative Appeals Chamber decision by Judge Brunner on 3 May 2024.
If you hold certain information, you should contact OFSI as soon as practicable.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
Explains requirements of the Town and Country Planning (Environmental Impact Assessment) Regulations 2017.
Read the Council Directive 2003/48/EC of 3 June 2003 on taxation of savings income in the form of interest payments.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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.
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