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The review of the safety of isotretinoin has concluded.
Information and advice for businesses on how to comply with consumer protection law in the online reviews and endorsements sectors.
Information for businesses on how to comply with consumer protection law on online reviews and endorsements.
A call for information on the use of online reviews and endorsements.
As a planning authority, find out how to review applications that might affect protected sites and areas.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Learn how the Government Digital Service is monitoring accessibility under the Public Sector Bodies (Websites and Mobile Applications) (No.2) Accessibility Regulations 2018.
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.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How investigators and sponsors should manage clinical trials during COVID-19
The Byelaws Review team is carrying out a far reaching overview and update of byelaws as they relate to all MOD sites in the UK.
The Coal Authority is undertaking an emergency review of all spoil tips in Wales.
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.
Explains how victims of persistent antisocial behaviour have the right to request a case review where a local threshold is met.
This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
This series brings together all documents relating to Section 28 Directions
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