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Drug Administration

Recor Medical and Otsuka Medical Devices Announce First FDA-Approved Renal Denervation System for the Treatment of Hypertension

Recor Medical, Inc. and its parent company, Otsuka Medical Devices Co., Ltd. (“Otsuka Medical Devices”) announced the U.S. Food and Drug Administration (FDA) has...

Werfen Receives US FDA 510(K) Clearance for Aptiva® Connective Tissue Disease Essential Reagent

Werfen, announced 510(k) clearance of Aptiva Connective Tissue Disease (CTD) Essential reagent by the US Food and Drug Administration (FDA). The Aptiva CTD Essential complements...

Egret Therapeutics Receives FDA Clearance of IND Application for EGT 101 for Treatment of Delayed Cerebral Ischemia

Egret Therapeutics, a clinical-stage biotechnology company focused on developing transformative therapies for neurological conditions, announced that the U.S. Food and Drug Administration (FDA) has...

ANeuroTech receives positive feedback from the FDA for its pivotal Phase IIIb development programme for ANT-01 as an adjunctive anti-depression drug for Major Depressive...

ANeuroTech, a leader in the development of innovative mental health treatments with minimal or no side effects, announces that following a successful pre-IND meeting,...

Medical Technologies Leader Cellmyx Announces U.S. Food and Drug Administration (FDA) 510(k) Clearance for intelliFat BOD

Cellmyx, the authority on autologous adipose grafting and transfer, and a leader in medical technologies for orthopedic physicians, pain management and regenerative medicine, announces...
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