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Maroc Maroc - DRUGS.COM - Pharma Industry News - 02/Jan 16:01

FDA Approves Symvess, an Acellular Tissue-Engineered Vessel

THURSDAY, Jan. 2, 2025 -- The U.S. Food and Drug Administration has approved Symvess, the first acellular tissue engineered vessel indicated for use in adults as a vascular conduit for extremity arterial injury when urgent revascularization is...

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SYMVESS (acellular tissue engineered vessel) implant [Humacyte Global, Inc.]

nlm.nih.gov - 30/12/2024 05:00

Updated Date: Mon, 30 Dec 2024 00:00:00 EST

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SYMVESS (acellular tissue engineered vessel) implant [Humacyte Global, Inc.]

nlm.nih.gov - 30/12/2024 05:00

Updated Date: Mon, 30 Dec 2024 00:00:00 EST

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FDA Approves Subcutaneous Opdivo Qvantig for Most Solid Tumor Indications

drugs.com - 03/Jan 16:01

FRIDAY, Jan. 3, 2025 -- The U.S. Food and Drug Administration has approved Opdivo Qvantig (nivolumab and hyaluronidase-nvhy) injection for...

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FDA Approves Subcutaneous Opdivo Qvantig for Most Solid Tumor Indications

drugs.com - 03/Jan 16:01

FRIDAY, Jan. 3, 2025 -- The U.S. Food and Drug Administration has approved Opdivo Qvantig (nivolumab and hyaluronidase-nvhy) injection for...

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FDA Approves Gemtesa for Overactive Bladder in Men With BPH

drugs.com - 02/Jan 22:39

THURSDAY, Jan. 2, 2025 -- Gemtesa (vibegron) has been approved by the U.S. Food and Drug Administration for men with overactive bladder (OAB)...

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Monthly News Roundup - December 2024

drugs.com - 31/12/2024 22:12

FDA Approves Zepbound as the First Prescription Drug for Obstructive Sleep Apnea in Adults with Obesity On December 20, 2024, the U.S. Food and Drug...

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FDA approves first drug for sleep apnea treatment

knowridge.com - 30/12/2024 11:04

The U.S. Food and Drug Administration (FDA) has approved Zepbound, a prescription weight-loss medication, as the first drug specifically for treating...

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FDA Drafts New Recommendations for More Inclusive Pulse Oximeter Testing

drugs.com - 07/Jan 23:01

TUESDAY, Jan. 7, 2025 -- The U.S. Food and Drug Administration released draft guidelines on Jan. 6 proposing that manufacturers conduct larger, more...

Inogen receives FDA 510(k) clearance for SIMEOX 200 airway clearance device

news.medical.net - 06/Jan 11:18

Inogen, Inc., a medical technology company offering innovative respiratory products for use in the homecare setting, today announced that it has...

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Advocates Say FDA Guidance on Lead Levels in Baby Food Is Insufficient

drugs.com - 08/Jan 00:01

TUESDAY, Jan. 7, 2025 -- The first-ever U.S. Food and Drug Administration guidelines on lead in baby food are under fire from health experts who argue...