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The Review was set up to consider how the Human Rights Act is working in practice and whether any change is needed. The independent Panel submitted their report to the Deputy Prime Minister in October 2021.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
The AQuA Book is Government guidance about how to produce robust, fit for purpose analysis. It's for all analysts, analytical managers and commissioners.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The Commission was established on 17 July 2015 to review the Freedom of Information Act 2000 and was dissolved on 11 March 2016.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
FCDO travel advice for Argentina. Includes safety and security, insurance, entry requirements and legal differences.
UK and others call for action to uphold safety of journalists and media freedom.
The review of the safety of isotretinoin has concluded.
FCDO travel advice for the Dominican Republic. Includes safety and security, insurance, entry requirements and legal differences.
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