Seminar - Mississauga, Ontario, Canada
This webinar is intended to help you get familiar with FDA’s Quality System Regulations (cGMP) for medical devices including in vitro diagnostic medical devices. This webinar is further intended to provide guidance on the best practices for implementing 21 CFR Part 820 (QSRs), which helps assure that medical devices are safe and effective for their intended use.
Tuesday, April 28, 2015 (13:00 - 14:00)
Compliance Trainings, Mississauga, Ontario 44813, Canada
Phone: 4169154458
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