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Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Links to EU guidance, as it stood immediately before end of transition period.
How traditional herbal medicines and homeopathic medicines will be treated by the MHRA.
Neuraxpharm UK Ltd is recalling specific batches after retesting showed out of specification results. The tabled batches are being recalled as a precautionary measure after testing showed variability of the capsule contents beyond permitted levels.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Check if someone selling medicines online in Northern Ireland is allowed to do so by the Medicines and Healthcare products Regulatory Agency (MHRA)
Fresenius Kabi Limited have informed the MHRA of a packaging error with specific batches of Sodium Chloride Intravenous Infusion 0.9% Freeflex and Freeflex PLUS.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK patients.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Information on granted EAMS scientific opinions, including the public assessment report and treatment protocols.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Records that must be kept when supplying or administering veterinary medicines in the UK.
Manx Healthcare Ltd. has informed MHRA that they have identified a problem with the product packaging of the batch indicated in the table.
Legal requirements for the sale of veterinary medicines on the internet and the VMD Accredited Internet Retailer Scheme (AIRS).
The MHRA has re-issued this notification as Class 3 recall based on further assessment. Please note the new actions for healthcare professionals listed within the notification. Doncaster Pharma Limited have identified an error relating to the Braille printed on the...
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
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