Event : DHF, DMR, DHR and TF - Regulatory Documents Explained - Webinar By GlobalCompliancePanel http://www.rsc.org/events/detail/8911/DHF%2c%20DMR%2c%20DHR%20and%20TF%20-%20Regulatory%20Documents%20Explained%20-%20Webinar%20By%20GlobalCompliancePanel This is a feed for event : DHF, DMR, DHR and TF - Regulatory Documents Explained - Webinar By GlobalCompliancePanel Thu, 11 Sep 2014 13:13:13 +0100 8911 8911 http://www.rsc.org/events/detail/8911/DHF%2c%20DMR%2c%20DHR%20and%20TF%20-%20Regulatory%20Documents%20Explained%20-%20Webinar%20By%20GlobalCompliancePanel DHF, DMR, DHR and TF - Regulatory Documents Explained - Webinar By GlobalCompliancePanel Event dates: 11 April 2013<br/>Event summary: The FDA QSR and the Medical Device Directive specify certain records that should be included in your organization's quality system - Design History File (DHF), Device Master Record (DMR), Device His<br/>Event Venue: Online Training, Fremont, 94539, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00