What Does MDR Stand For?

MDR stands for Medical Device Reporting

MDR, or Medical Device Reporting, refers to the process by which manufacturers, importers, and healthcare professionals report adverse events, defects, or failures associated with medical devices to regulatory authorities. This reporting system is essential for monitoring device safety and effectiveness, ensuring timely actions are taken to protect public health. MDR is a critical component of post-market surveillance and regulatory compliance, facilitating the identification of potential issues and the implementation of necessary corrective measures.