FDA Clears First Blood Test Used in Diagnosing Alzheimer’s Disease
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FDA to Host Inaugural, Independent, Scientific Expert Panel Open to Public
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MHRA approves guselkumab for Crohn’s disease and ulcerative colitis
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Guidance: Rules for the sale, supply and administration of medicines
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Medicines: reclassify your product
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Guidance: MORE implementation
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Manufacturer’s Online Reporting Environment (MORE)
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FDA Advances Robust, Transparent Post-Market Chemical Review Program to Keep Food Supply Safe and Healthy
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MHRA approves vaccine to protect against pneumococcal infections such as pneumonia and meningitis
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Thiopurines and intrahepatic cholestasis of pregnancy
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Register a homeopathic medicine
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Decision: Advertising Investigations: April 2025
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Decision: Medical devices given exceptional use authorisations during the COVID-19 pandemic
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Field Safety Notices: 5 to 8 May 2025
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Meet the women helping ensure that digital mental health technologies are safe, effective and developed considering the needs of the people who use them
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FDA Begins Action To Remove Ingestible Fluoride Prescription Drug Products for Children from the Market
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HHS, FDA Initiate Comprehensive Review of Nutrients in Infant Formula
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HHS, FDA Issue RFI on Deregulatory Plan to Lower Costs and Empower Providers
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Decision: Orphan registered medicinal products
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Class 4 Medicines Notification, Chemidex Pharma Ltd, Various Products, EL(25)A/21
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Decision: Parallel import licences granted in 2025
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Guidance: International Recognition Procedure
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Decision: Marketing authorisations granted in 2025
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MHRA approves first UK treatment for congenital thrombotic thrombocytopenic purpura (cTTP)
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Medicines: apply for a parallel import licence
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