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Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
How UK citizens or residents can get healthcare when visiting countries or territories outside the EU where the UK has reciprocal healthcare agreements.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Submission dates and how the submissions using the EC decision reliance procedure work.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Employment Appeal Tribunal Judgment of Jason Coppel Deputy Judge of the High Court on 24 April 2024.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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 .
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).
Information on requesting medical records held by the Ministry of Defence (MOD) for deceased service personnel.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance for industry and organisations to follow from 1 January 2021.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
Find out about the symptoms of COVID-19, what to do if you or your child has them and when to get medical help.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How investigators and sponsors should manage clinical trials during COVID-19
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Using an ecological momentary assessment to evaluate your digital health product.
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