What FDA-Regulated Industry Should Know about FDA’s New Policy on GMP Enforcement
January 31, 2019 - Online Event ON CAWebinar Compliance
info@webinarcompliance.com
Phone:4169154458
There are many things the FDA-regulated industry—including medical device manufacturers and professionals—should know about the FDA’s current inspection policy to adequately implement the good manufacturing practices (GMPs). The consequences of failing to comply with FDA regulations can lead to such severe civil and criminal actions, that you simply can’t afford to take them lightly. Learn the nuts and bolts of establishing GMPs for medical devices in this session by regulatory expert David Lim. Lim will discuss the critical factors you should consider when establishing design control. He will walk you through the common mistakes companies make, and show you how to avoid them. He will also be providing practical, actionable, sustainable solutions in an integrated, thorough manner (PASS-IT).