This seminar / workshop will examine the existing and proposed requirements for the U.S. FDA's DHF -- including its derivative documents, the DMR and DHR. It will consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes / goals, their similarities, as well as the two different device classification schemes.
The DHF, Technical File and Design Dossier - Similarities, Differences and The Future
28 - 29 August 2014, Las Vegas, United States
Introduction
Venue
Hilton Grand Vacations Suites at the Flamingo
Hilton Grand Vacations Suites at the Flamingo, 3575 Las Vegas Boulevard South, Las Vegas, Nevada, 89109-4313, USA, Las Vegas, 89109-4313, United States
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Organised by
GlobalCompliancePanel
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