by MDP Staff | Jul 24, 2025 | EU MDR, FDA Reports, Global-RA, Industry Information, MDR - Medical Device Report, Med-Devices, US-FDA
Global Medical Device Reporting and Vigilance Reporting serious safety risks Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact International Medical Device Reporting Medical Device Reporting and...
by MDP Staff | Jul 24, 2025 | FDA Reports, Industry Information, MDR - Medical Device Report, Quality system, Safety, US-FDA
FDA Medical Device Reporting Know when and how to file an MDR Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact U.S. FDA Medical Device Reporting What is 21 CFR Part 803 (Medical Device...
by MDP Staff | Jul 15, 2025 | Alerts, Alerts-Device, Class I Recalls, FDA Reports
BD Alaris Pump Module model 8100 Performance can worsen when connected to other perfusion sets Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Class I Recall (Correction) The FDA has issued an...
by Devices and Pharma | Apr 18, 2024 | FDA Public Information, FDA Reports, Industry News, Med-Devices, Product-Innovation, US-FDA
CDRH Issues its 2024 Innovation Report Commitment to medical device innovation and safety Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact Revolutionizing Medical...
by Devices and Pharma | Apr 18, 2024 | FDA Reports, Industry News, Med-Devices, Product Safety, US-FDA
CDRH Issues its 2024 Safety Report Commitment to safety and effectiveness of medical devices Home About Consumer Medical Devices Pharma Biologics Biologics Warning Letters AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact 2024 CDRH Safety...
