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Data, Freedom of Information releases and corporate reports
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.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
You’re disabled under the Equality Act 2010 if you have a physical or mental impairment that has a 'substantial' and 'long-term' negative effect on your ability to do daily activities
Rules you must follow, who’s responsible, when to tell the Environment Agency and what to do if you get an enforcement notice.
Find out about cover policy and indicators for countries and territories that are covered by UK Export Finance.
Employment Appeal Tribunal Judgment of Judge Tayler on 12 April 2024.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for childminders, nannies and other registered childcare providers with examples of what Ofsted considers to be a significant event.
How to identify and record the people who own or control your company.
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Agree the value of shares if you operate Enterprise Management Incentives or a Share Incentive Plan, or if you have Company Share Option Plans or Save As You Earn share schemes.
Find out about the VAT liability of insurance transactions and insurance related services.
Insuring an insolvent's property.
How a competent authority must decide if a plan or project proposal that affects a European site can go ahead.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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