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Clinical data management
Results: 1569

#	Item
541	18 July[removed]MEETING REPORT ICH Steering Committee June 5-6, 2013, La Hulpe, Brussels, Belgium Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-11-11 11:03:12 Research Clinical Data Management Medical informatics Pharmaceuticals policy Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA Electronic Common Technical Document La Hulpe Medicine Clinical research Health
542	Microsoft Word - ICH SC Meeting Chicago Summary Final, August 16, 2006.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-11-11 11:03:12 Science Pharmaceutical sciences Clinical Data Management Pharmaceuticals policy Pharmaceutical industry MedDRA Electronic Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Common Technical Document Clinical research Research Pharmacology
543	ICH STEERING COMMITTEE[removed]June 2011 Cincinnati, OH, USA SUMMARY 1. Opening Discussions The ICH Steering Committee (SC) meeting in Cincinnati was chaired by FDA. The Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-11-11 11:03:12 Electronic Common Technical Document Pharmaceutical industry MedDRA Environmental Working Group Quality by Design Common Technical Document International Organization for Standardization International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical Data Management Clinical research Research
544	Microsoft Word - ICH SC Meeting Brussels 2008-summary.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-11-11 11:03:12 Science Health Pharmaceuticals policy Drug safety Clinical Data Management International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA Electronic Common Technical Document Environmental Working Group Clinical research Research Pharmacology
545	Map Metadata – Going Beyond the Obvious/Connecting the Dots Gregory Steffens Associate Director, Technology Innovations Novartis Pharmaceuticals Add to Reading List Source URL: www.pharmasug.org Language: English - Date: 2014-10-29 10:15:34 Standards organizations Medical informatics Research Clinical trials Clinical Data Interchange Standards Consortium Nonprofit technology SDTM Metadata Database Information Data Clinical Data Management
546	Building (and Rebuilding) the CDISC Toolbox Background Frank Dilorio, Jeff Abolafia Add to Reading List Source URL: www.pharmasug.org Language: English - Date: 2014-10-12 18:56:03 Statistics Clinical Data Management Medical informatics Standards organizations Clinical research Clinical Data Interchange Standards Consortium SDTM Metadata XML Computing Technical communication Technology
547	Business & Decision Life Sciences CDISC Workshop: From SDTM to ADaM: Mapping Methodologies Jessica Minkue Mi Edou / 18th September 2014 Add to Reading List Source URL: www.phusewiki.org Language: English - Date: 2014-10-01 05:41:52 Medical informatics Standards organizations Clinical research Clinical trials Clinical Data Interchange Standards Consortium SDTM Clinical data acquisition Data set Statistics Clinical Data Management Research
548	Data Mining the Clinical Ecosystem Joshua Haznedar gRED - Development Sciences PhUSE SDE San Francisco September 26, 2014 Add to Reading List Source URL: www.phusewiki.org Language: English - Date: 2014-10-02 11:10:13 Data management Spotfire Biomarker Data mining Laboratory information management system R Science Medicine Data analysis
549	Assessment of the functioning of the „Clinical Trials Directive“ [removed]EC RE: Public Consultation Paper (ENTR/F/2/SF D[removed]CliniGene-NoE comments Jan 25th, 2010 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:24 Medicine Pharmaceutical sciences Pharmacology Pharmaceutical industry Clinical Data Management Clinical Trials Directive Common Technical Document Qualified Person Clinical trial Clinical research Research Pharmaceuticals policy
550	Managing Controlled Terminologies Across Clinical Lifecycle Stages A. Brooke Hinkson – Global Head, Clinical Information Governance Mihaela Simion – Manager, Metadata Curation Add to Reading List Source URL: www.pharmasug.org Language: English - Date: 2014-10-29 10:15:06 Research Standards organizations Clinical Data Management Clinical Data Interchange Standards Consortium Nonprofit technology Technology SDTM Information governance Metadata Medical informatics Data management Statistics

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