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Pfizer Limited is recalling all distributed batches of Oxbryta 500 mg Tablets. Pfizer Limited has informed the MHRA that the product is being withdrawn due to emerging data from clinical trials and registry-based studies.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
You must get permission to export certain drugs and medicines.
Information for companies on the import and export of controlled drugs to and from the UK.
How the MHRA makes decisions on what is a medicinal product (borderline products).
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Glenmark Pharmaceuticals Europe Ltd is recalling the affected batches as a precautionary measure due to out of specification results for unknown impurities during routine stability testing and additional re-testing.
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