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Medline Recalls Sub-G Endotracheal Tube

[ Price : $8.95]

Medline Industries recalls its Sub-G Endotracheal Tube with Subglottic Suction due to detachment or tearing of the inflation tube.

Concerns With Alzheimers Drug Development Guidance

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Biogen and Public Citizen call on FDA to address issues in its draft guidance on developing drugs to treat early Alzheimers diseas...

Women Underrepresented in Device Trials: Research

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Israeli researchers say more effort must be made to increase the number of women enrolled in medical device clinical trials.

Ipsen Gains Accelerated OK for Iqirvo

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FDA grants Ipsen accelerated approval for Iqirvo (elafibranor) 80 mg tablets for treating primary biliary cholangitis in combinati...

Obstetrics/Reproductive Advisory Panel Renewed

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Federal Register notice: FDA announces the renewal of its Obstetrics, Reproductive and Urologic Drugs Advisory Committee for an ad...

Arthritis Advisory Panel Renewed for 2 Years

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Federal Register notice: FDA announces the renewal of its Arthritis Advisory Committee for an additional two years.

Emerging Drug Safety Technology Meeting Program

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FDA launches an Emerging Drug Safety Technology Meeting (EDSTM) program to assist industry in implementing artificial intelligence...

GSKs Arexvy Gets Expanded Approval

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FDA approves an expanded use for GSKs Arexvy (respiratory syncytial virus vaccine, adjuvanted) for preventing RSV lower respirator...

FDA Clears 2 Abbott OTC Glucose Monitors

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FDA clears two Abbott 510(k)s for over-the-counter continuous glucose monitoring systems Lingo and Libre Rio.

FDA Panel Backs Lillys Alzheimers Drug

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FDAs Peripheral and Central Nervous System Advisory Committee unanimously votes to recommend the approval of Eli Lillys donanemab-...