Overview: This webinar is intended to demonstrate how to define, document, implement, and maintain the necessary procedures for medical device reporting. In the United States, since December 13, 1984, the Food and Drug Administration (FDA) Medical Device Reporting (MDR) regulations have required firms who have received complaints of device malfunctions, serious injuries or deaths associated with medical devices to notify FDA of the incident. MDR is the mechanism for the FDA to receive significant medical device adverse events from manufacturers, importers and user facilities, so they can be detected and corrected quickly. It is critical to understand how to define, document, implement, and maintain the procedures for MDR. This webinar will greatly help device industry and relevant professionals understand how to define, document, implement, and maintain the procedures for MDR. Why Should You Attend: IDevice manufacturers are required to establish and maintain a medical device adverse event reporting system, commonly known as Medical Device Reporting. This webinar will demonstrate how to define, document, implement, and maintain the necessary procedures for medical device reporting. Price: $225.00GlobalCompliancePanelUSA Phone:800-447-9407Fax: 302-288-6884