Seminar - Online
This webinar will provide valuable guidance to regulated companies in development and implementation of formal, defined, documented methods for analysis of product changes and when to file a new 510(k). Consideration of the U.S. FDA's current K-97-1 Memo / guidance document on "510(k) Device Modifications"
31 March, 2015 (13:00 - 14:30)
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Online
Email: suzzane.d@compliancetrainings.com
Phone: 4169154458
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