by Devices and Pharma | May 3, 2024 | FDA Approvals, Industry News, New Drugs, New Pharma Products, Pharmaceuticals, Product-Innovation, US-FDA
Drug Innovation - Tisotumab vedotin-tftv, marketed as Tivdak For Recurrent or Metastatic Cervical Cancer Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact Product Approval for Cervical Cancer Drug Exciting...
by Devices and Pharma | May 3, 2024 | Consumer Information, FDA Approvals, Industry News, New Drugs, New Pharma Products, Pharmaceuticals, Product-Innovation, US-FDA
FDA Drug Innovation - Anktiva Treatment of BCG-unresponsive non-muscle invasive bladder cancer (NMIBC) Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact New Drug Approval In a significant development for...
by Devices and Pharma | May 3, 2024 | Alerts, Alerts-Pharma, Consumer Information, Consumer Safety, FDA Safety Communication, Industry News, Pharmaceuticals, US-FDA
FDA Health Alert Regarding Rare Pregnancy Complication Risk of intrahepatic cholestasis of pregnancy (ICP) Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact FDA Safety Communication In a recent health safety...
by Devices and Pharma | May 2, 2024 | Alerts, Alerts-Device, Consumer Information, Consumer Safety, FDA Safety Communication, Industry Information, Industry News, Med-Devices, Product Safety, US-FDA
FDA Safety Communication - Exactech Equinoxe Shoulder System Potential risks with products packaged in defective bag Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact FDA Safety Communication April 19...
by Devices and Pharma | Apr 29, 2024 | Alerts-Device, Class I Recalls, Industry News, Med-Devices, MedWatch-System, Product Recalls, Product Safety, US-FDA
SonarMed Inc. Recalls Airway Acoustic Sensors Restriction of inner diameter may impede catheter passage Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact Urgent Class I Recall Notice SonarMed Inc. has issued...
by Devices and Pharma | Apr 28, 2024 | Device_Submissions, Industry Information, Med-Devices, New devices, Premarket-Notification-510(k), Reg_Information, US-FDA
Understanding the 510(k) Premarket Notification Learn how the FDA’s 510(k) premarket notification system facilitates the introduction of new medical devices to the market, ensuring safety and compliance. Explore Our Services Streamlining FDA Approval Get Expert...
