Biotech China 2014
Webinar on Quality System Regulations (QSRs) for Medical Devices and IVDs


Mississauga, Ontario
https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1351
Quality System Regulations, Medical Devices, IVDs, capa quality system , 21 CFR Part 820, cGMP requirements, Design History File, CAPA  Complaint Files, Design Transfer, Medical device  Design Validation, Medical device Design Verification, PMA approval requirements, Device History Record, Device Master Record, Medical Design Review, fda medical device approval process, cgmp compliance, cgmp for medical devices, medical devices compliance

Schedule of Presentations:

Tuesday, August 26, 2014
4th Annual Pharma R&D Asia Congress
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