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Dr Nicola Rose, Executive Director of Science and Research at the Medicines and Healthcare products Regulatory Agency (MHRA), has been appointed an OBE in the 2026 King’s Birthday Honours, for services to science and public …
As with any medicine, the MHRA will keep the safety and effectiveness of the adrenaline nasal spray under close review.
Having met the MHRA’s rigorous standards of safety, quality and effectiveness, the semaglutide tablet has been approved in the UK for weight loss and weight management.
The MHRA is publishing the results of an extensive public consultation which will inform the recommendations of the AI Commission and future regulations.
The London sandbox is a secure environment designed to safely test AI-enabled devices in a real-world environment so patients can benefit more quickly.
New AI sandbox will help make medicines safer, speed up development, and reduce reliance on animal testing.
As with all medicines, the MHRA will keep the safety and effectiveness of Nipolcalimab under close review.
Avacopan is used in the treatment of some rare autoimmune diseases affecting small blood vessels.
The adjuvanted trivalent influenza vaccine works by stimulating the immune system to produce its own protection against flu.
Resmetirom is used in adults who have experienced inflammation and cell damage, resulting in scarring.
The raid on a Northamptonshire estate dismantled what is believed to be a major illicit manufacturing and distribution operation
As with any medicine, the MHRA will keep the safety and effectiveness of rilzabrutinib under close review.
Patients taking Crescent Pharma Limited Ramipril 2.5mg capsules are advised to check their packaging for batch number GR155023 and contact their pharmacy if any blister strips inside are labelled as Ramipril 10mg.
Jason is an experienced technology leader with over 25 years working in tech leadership and health informatics.
Essential advice on protecting your medicines during extreme heat and staying safe.
The MHRA launches public consultation on new framework that could lead to earlier licensing for therapies for up to 3.5 million people in the UK.
Proposed Rare Disease Therapies Framework introduces Investigational Marketing Authorisation and compressed development pathways – industry urged to respond
MHRA announces new programme of events and greater engagement with industries, researchers, local NHS and government in Wales.
Innovation doesn’t wait for the rules to catch up. The question is whether we can build a system agile and flexible enough to keep pace.
As with any medicine, the MHRA will keep the safety and effectiveness of Vyjuvek under close review.
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