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A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Employment Appeal Tribunal Judgment of Judge Susan Walker, Mr Nick Aziz and Mr Steven Torrance on 25 March 2024.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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.
Submission dates and how the submissions using the EC decision reliance procedure work.
Besins Healthcare (UK) Ltd has informed the MHRA that a defective pump system was detected in two batches of Oestrogel Pump-Pack 750 micrograms/actuation Gel.
Using an ecological momentary assessment to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to write up and share your findings
Volume 37 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Volume 36 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 32 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 40 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Advice for investigators and sponsors of ongoing clinical investigations.
This guidance provides information on COVID-19 in homelessness, domestic abuse refuge, respite room and asylum seeker accommodation settings.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Volume 45 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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