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Food and Drug Administration / Pharmacology / Clinical Data Management / Clinical trials / Clinical Data Interchange Standards Consortium / SDTM / SAS / Pharmaceutical industry / Data quality / Statistics / Research / Clinical research


automated, replicable CDISC conversion Clinical Trial Data: Automated, Replicable CDISC Conversion Synopsis + IND and NDA programs necessitate recurrent submission of clinical trial data to regulatory agencies in specif
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Document Date: 2015-02-18 15:13:15


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File Size: 207,64 KB

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