We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use °Ç¸ç³Ô¹Ï, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Help improve °Ç¸ç³Ô¹Ï
As with any medicine, the MHRA will keep the safety and effectiveness of deuruxolitinib under close review.
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…
Do not include personal or financial information like your National Insurance number or credit card details.
To help us improve °Ç¸ç³Ô¹Ï, we’d like to know more about your visit today. .