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Design History Files, Device Master Records, Device History Records, and Technical Files in Medical Industry

21 February 2012, Palo Alto, United States


Introduction
This webinar will discuss in detail the existing and proposed requirements for the FDA's DHFs, DMRs, DHRs and the MDD's TF/DD.

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Venue
Online Event

Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States

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Organised by
ComplianceOnline
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