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2 Day Seminar: Managing Your Complaints and Obstacles in Post-Market Requirements - Results from Top Medical Device Observations During an Inspection (Pittsburgh, United States - May 3-4, 2018) - ResearchAndMarkets.comThe "Managing Your Complaints and Obstacles in Post-Market Requirements - Results from Top Medical Device Observations During an Inspection" conference has been added to ResearchAndMarkets.com's offering. This course will provide an understanding of MDR & recall compliance and the interrelationship of Complaint Handling, CAPA, and Risk Management processes. It will be beneficial to all device manufacturers and is recommended for any individuals or teams that are involved in medical device reporting (MDR) and correction & removal processes, including recalls. The FDA is continuing their efforts to issue numerous FDA Warning Letters and serious enforcement actions, including criminal & civil penalties levied on companies that failed to properly report events and take proper corrective and removal actions. The number of device companies having their recall classified as a Class 1 (most severe) ecall has surged in the past three years. Additionally, product liability and financial risks are staggering when companies fail to properly report and take action when required. Agenda Day One (8:30 AM - 5:00 PM)
Day Two (8:30 AM - 4:00 PM)
For more information about this conference visit https://www.researchandmarkets.com/research/3pb4fh/2_day_seminar?w=4 View source version on businesswire.com: https://www.businesswire.com/news/home/20180410006325/en/ |