Recent focus has been placed on the medical device industry in reviewing its capacity to evaluate, monitor and alert users of safety concerns related to the specific devices. Although significant efforts are underway to change this and facilitate sounder medical device reporting and electronic medical device reporting, companies are still struggling with identifying what the international and national regulatory bodies are requiring.

This timely conference will bring together Regulatory & Quality professionals to address key updates and advancements in medical device safety, medical device reporting, eMDR, post market-surveillance, complaint handling, audit handling, and national & international standards.