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U.S. Medical Device Reporting

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...

Mechanical Circulatory Support (MCS) Devices

by Devices and Pharma | Jul 10, 2025 | Cardiovascular, Implantable Devices, Industry Information, Med-Devices, Products_Devices

Mechanical Circulatory Support (MCS) Devices Product family overview Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact Overview of MCS Devices Mechanical Circulatory...

China Implements a Ban on European Medical Devices

by Devices and Pharma | Jul 8, 2025 | Global-RA, Industry Information, Industry News

China Retaliates Against European Union Device Manufacturers Imposes a ban on European medical devices Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Growing China-EU Trade Conflict The medical...

Orthopedics Industry Consolidation

by Devices and Pharma | May 18, 2025 | Implantable Devices, Industry Information, Industry News, Orthopedics

Orthopedic Device Industry Consolidation Combining company assets Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Consolidation in the Implantable Orthopedics Industry: A Historical Perspective ...

How Unsafe Medical Devices Can Slip Through the Cracks

by Devices and Pharma | May 16, 2025 | Consumer Information, Industry Information, Med-Devices, MedWatch-System, Product Safety, Quality Information, Safety, US-FDA

Medical Devices Deemed Unsafe Overseas but Sold in the US A Global Gap in Patient Protection Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Healthcare professionals and the device industry share...

Study Reveals Delays in Medical Device Adverse Event Reporting

by Devices and Pharma | May 16, 2025 | Industry Information, Med-Devices, Product Safety, Regulatory_Info, Safety

Device Manufacturers Often Delay Reporting Adverse Events Four major manufacturers account for nearly half of late reports Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Healthcare professionals...
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