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Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
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.
Gerry Murphy was appointed as a non-executive board member of the Department of Health and Social Care in 2014 and chairs its Audit and Risk Committee. He is a co-opted member of the NHS England audit and risk assurance committee....
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
The Prisons and Probation Ombudsman (PPO) investigates complaints from prisoners, young people in detention (prisons and secure training centres), those on probation and individuals detained under immigration powers (detained individuals). It also investigates all deaths that occur among prisoners, young...
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Find contact details of panel deputies available to support people who lack mental capacity.
Find out how to submit brand details to HMRC for Scotch Whisky, Irish Whiskey, Irish Cream, Irish Poteen, Somerset Cider Brandy and Single Malt Welsh Whisky if you're a verified bottler.
Weights and Measures Act 1985 and subsequent Deregulation Order 1999 (as amended).
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to prepare for implementation and compliance of the Safety Features Regulation.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Employment Appeal Tribunal Judgment of Mr Justice Griffiths on 18 July 2024.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 19 July 2024, approved the first generic raltegravir medicines to treat adult and paediatric HIV patients who weigh at least 40kg.
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