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Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
Product recall for LCD Writing Tablet Doodle Board presenting a serious risk of injuries & choking as it contains a loose button cell battery.
From next month women in England can get their contraceptive pills without contacting their GP first.
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 Crescent Pharma Limited.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Teva UK Ltd. has informed the MHRA of a labelling error. This notification provides further advice on the safe use of the product.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Horse product from the USA seized at East Midlands Airport.
Information for patients, healthcare professionals and developers of new medicines
Torrent Pharma (UK) Limited is recalling certain batches of Ramipril 1.25mg tablets as a precautionary measure due to these batches having a low assay and high related substances test results after their release to the market.
Change to the information provided on adverse events in the SPC for Apoquel Film-coated Tablets for Dogs and Apoquel Chewable Tablets for Dogs.
Orifarm UK has informed the MHRA of an error with the Patient Information Leaflet (PIL) packaged within the parallel import packs of the specific batches of Concerta XL 18mg and 36mg prolonged release tablets mentioned in this notification.
Tillomed Laboratories Limited is recalling one batch of Labetalol 200mg Tablets due to an error on the foil blister packaging.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
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