Integrating the requirements of 21 CFR 820 into a product development process is challenging. Done poorly, it drags down the design process and puts you at risk. Done well, it delivers quality products, resource efficiencies and compliance that are easily demonstrated to the FDA.
Medical Device - QSR Compliant Product Development Process: One and half day In-person Seminar
23 January 2014, San Francisco, United States
Introduction
Venue
Grand Hyatt San Francisco, CA |
Grand Hyatt San Francisco, CA |, 345 Stockton Street, San Francisco, 94303, United States
Organised by
ComplianceOnline
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