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Tuesday, June 02, 2015
1:00 PM - 2:30 PM
1:00 PM - 2:30 PM See all dates and Times
https://www.complianceglobal.us/product/700098
This webinar will examine the existing and proposed requirements for the U.S. FDA's DHF per the CGMPs, 21 CFR 820.30 (j), including its derivative documents, the DMR and DHR.
