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How an innovative funding mechanism is saving lives by speeding up the availability of vaccines and making them affordable.
MHRA updates product information regarding the very rare risk of non-arteritic anterior ischemic optic neuropathy (NAION) in patients taking semaglutide.
There are changes to the legislation on reference medicinal products (RMPs) used to support abridged marketing authorisation applications.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Information on comparator products used in studies supporting abridged marketing authorisation application.
Guidance on conditional marketing authorisations, exceptional circumstances marketing authorisations and national scientific advice.
Guidance covering various aspects of pharmacovigilance for authorised and unauthorised medicinal products (Specials and the Early Access to Medicines Scheme (EAMS)).
How to apply for a clinical trial from 28 April 2026, including eligibility, documentation and registration in a public registry.
Notification on the Forensic Science Regulator’s press release following Greater Manchester Police’s statement of 29 November 2024 concerning suspected data manipulation at Randox Testing Services and Trimega Laboratories.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
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