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Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Marketing authorisations granted in 2024
Consumer advice and details of how to report problems with e-cigarettes with guidance on how to place an e-cigarette on the market in Great Britain and Northern Ireland, including the notification scheme.
Crescent Pharma Limited has informed the MHRA regarding an error with the European Article Number (EAN) barcode on the cartons of the above-mentioned batches of Pantoprazole 40 mg Gastro-Resistant Tablets distributed by Cres…
The tighter controls being introduced to minimise risk of overuse and or addiction of painkillers containing codeine or dihydrocodeine.
The Innovative Devices Access Pathway (IDAP) pilot is designed to accelerate the development of innovative medical devices that meet an unmet clinical need in the NHS and support their integration into the UK market.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
UK companies who have their licence to manufacture or wholesale medicines terminated and cancelled.
List of Field Safety Notices (FSNs) from 22 to 26 January 2024.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Information on MHRA's enforcement duties and how to report a non-compliant medical device.
Further detail on the arrangements giving effect to the Windsor Framework.
Disabling, long-lasting or potentially irreversible adverse reactions affecting musculoskeletal and nervous systems have been reported very rarely with fluoroquinolone antibiotics. Fluoroquinolone treatment should be discont…
How to contact MHRA for specific services or enquiries.
MHRA services & information for patients and healthcare professionals.
The MHRA have published a roadmap which outlines the intended timelines for delivering the future regulatory framework for medical devices.
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