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Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
A. Menarini Farmaceutica Internazionale Srl is recalling a specific batch as a precautionary measure due to the distribution of Invokana 300mg in Northern Ireland in packaging intended for the Greek market.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
How UK citizens or residents can get healthcare when visiting countries or territories outside the EU where the UK has reciprocal healthcare agreements.
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 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 Oct - 31 Dec 2023.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Volume 45 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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 get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Advice and guidance on the health needs of migrant patients from Uruguay for healthcare practitioners.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Volume 40 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
This is a list of all the opinions the RPC issued between 2015 and 2017 on Department of Health (DH) measures.
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