This webinar will provide valuable assistance to all regulated companies, since a CAPA program is a requirement across the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields.
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements in a Cost Effective Manner - Webinar By GlobalCompliancePanel
6 October 2011, Wilmington, United States
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online training webinar
online training webinar, 1000 N West Street, de, Suite 1200, Wilmington, 19801, United States
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global compliance panel
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