Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals - Webinar By ComplianceO (FDA GXP Compliance -)
Venue: Online Event
|Event Date/Time: May 23, 2012||End Date/Time: May 23, 2012|
The FDA's 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. Device firms are also subject to compliance to the FDA regulations of device recalls, reports of corrections and removals. To achieve compliance and to remain compliant, it is critical to understand how to define, document and implement the procedures for MDR, recalls, corrections and removals.
This webinar is aimed at helping device industry understand how to develop, maintain and implement the procedures for MDR, recalls, corrections and removals and further provide practical and actionable perspectives by increasing awareness and familiarity of the regulatory requirements.
At the end of the webinar, you will get empowered in a way that you would plan, develop, maintain and implement the relevant procedures efficiently and effectively.