
Study reports results from experiential HIV-testing education for nurses
A completed study evaluated whether experiential HIV-testing education could improve nurses' knowledge and testing practice while reducing stigma.
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A completed study evaluated whether experiential HIV-testing education could improve nurses' knowledge and testing practice while reducing stigma.
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ClinicalTrials.gov reports results from a completed post-approval study comparing Coflex with fusion for lumbar spinal stenosis.
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A completed Phase 2 study used dual MRI to investigate cardiopulmonary findings in people with persistent symptoms after COVID-19.
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ClinicalTrials.gov has posted results from a completed study of neurofeedback-enhanced mindfulness in traumatic brain injury.
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The authority said the first-stage transfer covers 60 family-health centres and units and seven hospitals in Minya.
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The regulator said inspection campaigns across 17 governorates led to closures and seizures of medicines and supplies of unknown origin.
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A completed Phase 1 study in 28 healthy Korean men reports pharmacokinetic measurements for single and repeated doses of apremilast.
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ClinicalTrials.gov has posted results from a completed Phase 4 study evaluating treatment approaches in smokers with asthma.
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The UK regulator has issued a safety notice concerning Class 4 Medicines Defect Notification, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 4 Medicines Defect Notification, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 4 Medicines Defect Notification, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 4 Medicines Defect Notification, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 3 Medicines Recall, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 4 Medicines Defect Notification, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 3 Medicines Recall, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning UPDATE, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 2 Medicines Recall, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 2 Medicines Recall, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 4 Medicines Defect Notification, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Class 4 Medicines Defect Notification, with guidance for affected healthcare services.
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The UK regulator has issued a safety notice concerning Dräger Atlan Anaesthesia workstations, with guidance for affected healthcare services.
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Using a standard IV infusion set instead of a blood-transfusion set may under-deliver blood or destroy red cells, potentially causing serious injury.
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Affected components in Kimal procedure packs carry risks of syringe disconnection or foreign particles and should be used only for urgent procedures when no alternative exists.
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Rare cases in which the balloon did not pass as intended have led to gastric outlet or bowel obstruction and gastric perforation, requiring prompt assessment.
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A sealed 2.5 mg carton from batch GR155023 contained two 10 mg blister packs, creating a risk of unintentional overdose, the UK regulator says.
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The recall covers specified 1 mL and 1.5 mL applicators after a packaging-process issue that could allow pathogen contamination and raise infection risk.
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Corrective action has allowed UK sales to resume, but transplant teams are told to inspect every bag for leakage, discoloration, particles or contamination before use.
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The regulator says specified devices lack valid UKCA or CE conformity evidence, so assurance of safety, sterility and performance cannot be fully guaranteed.
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A circuit-board fault can unexpectedly stop ventilation in Astral 100 and 150 devices made before October 2024, requiring immediate access to alternative ventilation.
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Batch 4L01372H is being recalled over possible small metal particles found during shelf-life testing; the MHRA says no harm reports had been received.
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