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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.
Insuring an insolvent's property.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to tax a beneficial loan arrangement for a director or employee.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find out about clearance applications and how to apply to HMRC for advance confirmation of an exempt distribution when a company purchases its own shares.
A guide to applying for compensation under the Criminal Injuries Compensation Scheme.
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Find out when you can zero rate books and other forms of printed matter.
Rules you must follow, who’s responsible, when to tell the Environment Agency and what to do if you get an enforcement notice.
Requirements for excise goods held in duty suspension in a warehouse by an authorised warehousekeeper, registered owner, duty representative or registered consignor in the UK.
Find out why you need to get a premises guarantee and how to get one.
How to identify and record the people who own or control your company.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Explains control of advertisement regime.
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