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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


Introduction
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.
Venue
Online

Compliance Trainings, Online, 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Mississauga, ON, Canada, Mississauga, ON, L5V 2V5, Canada

Organised by
Compliance Trainings
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