Biotech China 2014
Webinar on Robust Verification and Validation


Mississauga, ON, Canada - Ontario
https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1263
FDA Warning Letters,  cGMP deficiencies, ICH Q9, ISO 14971, quality management system, Robust Verification and Validation, Recent Regulatory requirements, product risk management factor, QMS V&V , 21 CFR Part 11, DQ, IQ, OQ, PQ, ASTM E2500 Equivalents, Hazard Analysis, FDA's Software V&V Model, Medical Devices, Pharmaceutical, Diagnostic, Biologics

Schedule of Presentations:

Wednesday, July 30, 2014
4th Annual Pharma R&D Asia Congress
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