This webinar will provide the new and expected guidances on data standards and electronic submissions for drugs and medical products. We will explain what are the policies and the requirements for submissions and standards for drugs in US and globally and how it affects healthcare/drug industry to adopt them.
e-Submissions & Data Standards for FDA (eCTD, CDISC, HL7) - Webinar By GlobalCompliancePanel
25 April 2013, Fremont, United States
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Online Training
Livermore Common, Online Training, California, Fremont, 94539, United States
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GlobalCompliancePanel
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