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Date: 2015-12-14 16:21:29Clinical research Pharmaceutical industry Clinical trials Design of experiments Food and Drug Administration Contract research organization Institutional review board Case report form Investigational device exemption Site management organization Clinical research coordinator Monitoring in clinical trials | Microsoft Word - MAGI_Model_CTA v1.07 Abbreviated.docAdd to Reading ListSource URL: magiworld.orgDownload Document from Source WebsiteFile Size: 152,00 KBShare Document on Facebook |
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