Biotech China 2014
Webinar On Key Regulatory Documents: Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) and Design Dossier


Mississauga, ON, Canada - Ontario
https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1261
Design History File, DHF, Device Master Record, DMR, Device History Record, DHR, Technical File, TF,  Design Dossier, Key Regulatory Documents, cGMPs mandate Design Control, DHF Compliance, Typical Technical File, Medical Devices, cGMP inspections, cGMP regulations, cGMP requirements

Schedule of Presentations:

Wednesday, July 16, 2014
4th Annual Pharma R&D Asia Congress
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