First Page | Document Content | |
---|---|---|
Date: 2012-11-26 09:44:41JMP Clinical trials SAS Clinical Data Interchange Standards Consortium SDTM Exploratory data analysis R Autoimmunity Statistics Food and Drug Administration Clinical research | Add to Reading ListSource URL: www.phusewiki.orgDownload Document from Source WebsiteFile Size: 91,54 KBShare Document on Facebook |
PDF DocumentDocID: 1pWCY - View Document | |
Department for Environment, Food and Rural Affairs Version 4.0 Document Reference: magi0057v4.doc MAGICDocID: 1aMiE - View Document | |
CDER / CBER Study Data Standardization Plan Recommendations ABC Pharma Company Study Data Standardization Plan 1. General Sponsor InformationDocID: 1a7qc - View Document | |
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 specifDocID: 18mMI - View Document | |
Microsoft Word - Basic Policy on e-studysubmit for NDA.docxDocID: 1855z - View Document |