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Read the draft text of notices that will be made under the provisions of The Customs (Export) (EU Exit) Regulations.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Top tech experts are meeting the Justice Secretary as part of a Government drive to use AI and technology to transform the justice system and cut crime.
'The Crown and suppliers: a new way of working’ event was held on 21 November 2011 in London.
Information for EU citizens and their families applying to the EU Settlement Scheme.
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
Don’t include personal or financial information like your National Insurance number or credit card details.
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