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As part of developing its new five-year strategy, the MHRA is publishing a series of blogs on the challenges and opportunities ahead. In the first instalment, Chief Executive Lawrence Tallon reflects on the changing healthca…
The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 16th September 2025, approved the medicine vorasidenib (Voranigo).
Patients implanted with affected devices should expect to be contacted directly for a follow-up assessment, if required.
More than 40 people hospitalised following suspected use of unlicensed botulinum toxin products.
As with any medicine, the MHRA will keep the safety of gepotidacin under close review.
As with any medicine, the MHRA will keep the safety of zuranolone under close review.
The pilot will help sponsors prepare for a new substantial modifications process under upcoming regulations, with responses delivered within 14 days.
Parents and caregivers who have purchased Nutrition Ignition Kids Magnesium Glycinate Gummies should stop giving them to children and safely dispose of any remaining product. It is recommended that advice be sought from a he…
As with any medicine, the MHRA will keep the safety and effectiveness of teplizumab under close review.
WHO recognition affirms MHRA’s commitment to regulatory excellence, innovation and global collaboration
The microscopic bacteria living in women’s bodies could be a powerful tool for personalised, non-invasive treatment and earlier diagnosis.
Under a joint information sharing agreement, pharmaceutical companies will be invited to register early with the MHRA and NICE to allow parallel decision making over licencing and value.
Updates on regulatory reform and plans to support innovation.
New jobs to strengthen innovation, safety and smarter regulation across the UK health and life sciences sector.
Due to risk of infection, non-sterile alcohol-free wipes are not appropriate for the treatment of injuries, wounds or on broken skin, nor for cleaning of intravenous lines.
Statement of Policy Intent sets out initial thinking on a new Early Access service to help patients benefit sooner from innovative medical devices that address unmet clinical needs.
The approval is supported by a study involving 453 adults with advanced platinum-resistant cancers of the ovary, fallopian tubes and the peritoneum that were FRα positive
New genetic therapy approved for SOD1-ALS brings targeted treatment option to patients in the UK
A new regional centre to promote Yellow Card reporting has been launched in Belfast today.
As the UK enters the heart of summer – with temperatures rising and families holidaying – the Medicines and Healthcare products Regulatory Agency (MHRA) is reinforcing essential safety advice for anyone using medicines or me…
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