May 08, 2025
Teleflex Secures FDA 510(k) Clearance for Broader Use of QuikClot Control+™ Hemostatic Device On April 30, 2025, Teleflex Incorporated, a global leader in medical technologies, announced that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the expanded Indications for Use ...
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A New Era for Multiple Myeloma Treatment: Bispecific Antibodies Enter the Fray
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LEQEMBI: A New Hope for Alzheimer’s Disease Patients
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