MDSAP Audits – All You Need to Know
December 12, 2018 - Online Event ON CAWebinar Compliance
info@webinarcompliance.com
Phone:1-416-915-4458
After the final FDA approval and initiation of marketing of your medical devices, regulating bodies such as US FDA and other regulatory bodies send their inspectors on a periodic basis to device manufacturing facilities. Now, the new MDSAP, Medical Device Single Audit Program can reduce the frequency and length of these audits. This important and timely webinar will discuss the key preparation steps for MDSAP of your medical device manufacturing quality system.
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