Dir, Post Market Surveillance
Cook Incorporated
Larry Pool has over 20 years of experience in the medical device industry. He has worked in various roles of regulatory, quality and operations for class I, II and III medical device manufacturers. The majority of his work has been focused on adverse event reporting, field actions, and post market surveillance. Larry has submitted several 510(k) submissions and product registrations in multiple countries. He has supported and led remediation efforts for CAPAs, 483s and warning letter responses. Currently, Larry is the Director of Post Market Surveillance for Cook Incorporated.
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US Regulatory Essentials for Devices and IVDs
Tuesday, October 3, 2023
8:30 AM – 4:00 PM EDT