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As with any medicine, the MHRA will keep the safety and effectiveness of imlunestrant tosylate under close review.
As with any medicine, the MHRA will keep the safety and effectiveness of brensocatib under close review.
Zanidatamab is used when the cancer cannot be removed by surgery and has spread to nearby tissues or other parts of the body.
As with any medicine, the MHRA will keep the safety and effectiveness of Nirogacestat hydrobromide under close review.
As with any medicine, the MHRA will keep the safety and effectiveness of lenacapavir under close review.
As with any medicine, the MHRA will keep the safety and effectiveness of depemokimab under close review.
As with any medicine, the MHRA will keep the safety and effectiveness of fluticasone propionate under close review.
As with any medicine, the MHRA will keep the safety and effectiveness of mirdametinib under close review.
As with any medicine, the MHRA will keep the safety and effectiveness of concizumab under close review.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 16th September 2025, approved the medicine vorasidenib (Voranigo).
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.
As with any medicine, the MHRA will keep the safety and effectiveness of teplizumab under close review.
New measures to crack down on cowboy cosmetic procedures will be introduced by the government.
First published during the 2024 to 2026 Starmer Labour government
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
Ensuring the seasonal flu vaccine is ready, safe and effective involves months of international planning, testing and collaboration
The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 18 July 2025, approved adrenaline (epinephrine) nasal spray (EURneffy) to be used for the emergency treatment of serious allergic reactions, known as …
The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 8 July, become the first regulator in the world to approve elinzanetant (Lynkuet) for the treatment of moderate to severe vasomotor symptoms (hot flus…
The new Business Plan sets out priorities for 2025–26: Protecting public safety and maintaining public trust; delivering efficient, predictable services through regulatory excellence; being an agile organisation that drives …
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