http://www.rsc.org/events/detail/6975/Design%20History%20File%20(DHF)%2c%20Device%20Master%20Record%20(DMR)%2c%20Device%20History%20Record%20(DHR)%20and%20Technical%20File%20(TF)%20-%20Regulatory%20Documents%20Explained%20-%20Webinar%20By%20GlobalCompliancePanel This is a feed for event : Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained - Webinar By GlobalCompliancePanel Thu, 11 Sep 2014 13:13:13 +0100 6975 6975 http://www.rsc.org/events/detail/6975/Design%20History%20File%20(DHF)%2c%20Device%20Master%20Record%20(DMR)%2c%20Device%20History%20Record%20(DHR)%20and%20Technical%20File%20(TF)%20-%20Regulatory%20Documents%20Explained%20-%20Webinar%20By%20GlobalCompliancePanel Event dates: 14 February 2012<br/>Event summary: Overview: The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Mas<br/>Event Venue: OnlineTraining, Wilmington, 19801, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00