This 90 minute webinar will examine the existing and proposed requirements for the U.S. FDA's DHF and the EU MDD's TF/DD.
Webinar On Key Regulatory Documents: Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) and Design Dossier
16 July 2014, Mississauga, ON, Canada
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Compliance Trainings, Online, 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Mississauga, ON, Canada, Mississauga, ON, L5V 2V5, Canada
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