Biotech China 2014
Webinar On FDA Inspection and Medical Device Design Control


Mississauga, ON, Canada - Ontario
https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1352
FDA Inspection, Medical Device Design Control, FDA warning letters, FDA enforcement trends, 21 CFR 820.30, adequate design control procedures, medical devices, design control requirements, design control system requirements, regulatory compliance, Medical devices IVDs, IVD firms, Design Verification And Validation, Governing Medical Devices Regulations, Design History File, Device History Record, Device Master Record

Schedule of Presentations:

Tuesday, July 15, 2014
4th Annual Pharma R&D Asia Congress
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