We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, 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
Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
Employment Appeal Tribunal Judgment of Jason Coppel Deputy Judge of the High Court on 24 April 2024.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Employment Appeal Tribunal Judgment of Mrs Justice Eady on 18 April 2024.
How UK citizens or residents can get healthcare when visiting countries or territories outside the EU where the UK has reciprocal healthcare agreements.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Information on requesting medical records held by the Ministry of Defence (MOD) for deceased service personnel.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Bristol-Myers Squibb Pharmaceuticals Limited has informed the MHRA that a potential product quality issue has been detected, relating to incomplete crimping of the metal crimp cap of OPDIVO 10mg/mL concentrate for solution for infusion (nivolumab) (1VLX10ML).
Provides shipowners with links to information to maintain awareness of hazards and risks which are causing accidents to inform risk assessments and procedures.
Provisional monthly HES
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Advice and guidance on the health needs of migrant patients from Senegal for healthcare practitioners.
medac GmbH (t/a medac Pharma LLP) is recalling the product for the batch specified in this notification due to particles detected during long-term stability tests.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Advice and guidance on the health needs of migrant patients from Argentina for healthcare practitioners.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.