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Register to vote Register by 18 June to vote in the General Election on 4 July.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
How veterinary medicines can be advertised.
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.
Desitin Pharma UK Ltd is recalling all batches of Lamotrigine Desitin 10mg/ml Oral Suspension as a precautionary measure due to an out of specification observation in the appearance of samples during routine stability testing. Please note this is a Class...
When entering the UK, you need to prove your medicine is prescribed to you if it contains a controlled drug - find out what proof you need to get.
The Medicines and Healthcare products Regulatory Agency’s (MHRA) Criminal Enforcement Unit (CEU) seized hundreds of thousands of doses of suspected illegally traded medicines, including powerful prescription-only medicines, following coordinated raids at two residential and two business premises across North Manchester.
Advice on best practice for reviewing individuals in substance misuse treatment.
Your rights and security searches, body scans and privacy rules if you're disabled or taking medication aboard aircraft
Cygnus Pharma Ltd. Have informed MHRA that the European Article Number (EAN) barcode printed on various packs of Trazodone Hydrochloride 50mg/5ml Oral Solution, is defective and returns the incorrect information.
You must get permission to export certain drugs and medicines.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Accord Healthcare Ltd, UK has informed the MHRA about an error with the Patient Information Leaflets (PILs) that have been packaged in the batches of these products mentioned in this notification.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance for prescribing vets on the use of the cascade.
There is a risk of harmful drug interactions with the ritonavir component of the COVID-19 treatment Paxlovid▼ due to its inhibition of the enzyme CYP3A, which metabolises many commonly used drugs. Prescribers should obtain a detailed patient history of current...
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
A 4-year Retrospective Study at a Tertiary Cancer Center, Kerala, India
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