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Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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.
The guidance and forms you need to import a human medicine into the UK, including unlicensed medicines.
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 .
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
The CMA is investigating Microsoft Corporation’s (Microsoft) hiring of certain former employees of Inflection AI, Inc. (Inflection AI) and its entry into associated arrangements with Inflection AI.
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).
Advice and guidance on the health needs of migrant patients from Argentina for healthcare practitioners.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Information on taking, submitting and processing samples which potentially contain monkeypox virus.
How to apply for marketing authorisation via this new procedure.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Advice and guidance on the health needs of migrant patients from Senegal for healthcare practitioners.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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