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Register to vote Register by 18 June to vote in the General Election on 4 July.
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.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
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.
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.
A Guide for Employers and Employees to the role of the Central Arbitration Committee (CAC) for these regulations
The review of the safety of isotretinoin has concluded.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out what information accountable persons must provide to different individuals and organisations and when to transfer it.
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