CPI™ Certification as Predictor of Clinical Investigators’ Regulatory Compliance (English)
- New search for: Vulcano, David M.
- New search for: Vulcano, David M.
In:
Drug information journal : DIJ / Drug Information Association
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46
, 1
; 84-87
;
2012
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ISSN:
- Article (Journal) / Electronic Resource
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Title:CPI™ Certification as Predictor of Clinical Investigators’ Regulatory Compliance
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Contributors:Vulcano, David M. ( author )
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Published in:Drug information journal : DIJ / Drug Information Association ; 46, 1 ; 84-87
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Publisher:
- New search for: Springer International Publishing
- New search for: Sage
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Place of publication:Thousand Oaks, Calif.
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Publication date:2012
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ISSN:
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ZDBID:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
- New search for: 44.00 / 44.40
- Further information on Basic classification
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Table of contents – Volume 46, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 5
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Editor-in-Chief’s Commentary: SAGE Publishes the Drug Information JournalTurner, J. Rick et al. | 2012
- 7
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The Ditchley Transparency ManifestoLofstedt, Ragnar / Bouder, Frederic et al. | 2012
- 8
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An In-Process Scaling Model: A Potential Framework for Data Monitoring Committees and Clinical Trial Quality ImprovementSmith, Alan / Seltzer, Jonathan et al. | 2012
- 13
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Flexible Phase I Study Designs: Expediting Early Clinical Drug DevelopmentUnderwood, David et al. | 2012
- 19
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Exposure to and Understanding of Technical Terms in Informed Consent Forms for Biomedical ResearchJeong, Ihn Sook / Kim, Dong-Hee / Kim, Myunghee / Kim, So Hee / Jeong, Dongwook / Shon, Ji Hong et al. | 2012
- 27
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Patient Nonadherence in Clinical Trials: Could There Be a Link to Postmarketing Patient Safety?Smith, Dorothy L. et al. | 2012
- 35
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Improving Time to Pharmaceutical Approval: An Analysis of the Prescription Drug User Fee Act ProcessMasciale, Andrea C. / DeSantis, Patricia L. / Siegel, Jay P. et al. | 2012
- 43
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Experiences With the Approval of Clinical Trials in Germany: Results of a Survey of Research-Based Pharmaceutical CompaniesRuppert, Thorsten / Pfeiffer, Boris Mirko et al. | 2012
- 57
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An Appraisal of Good Regulatory Review Practices in the Gulf Cooperation Council StatesAl-Essa, Reem / Salek, Sam / Walker, Stuart et al. | 2012
- 65
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Regulatory Review Process in the Gulf Cooperation Council States: Similarities and DifferencesAl-Essa, Reem / Salek, Sam / Walker, Stuart et al. | 2012
- 73
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Development and Application of Scorecards to Assess the Quality of a Regulatory Submission and Its ReviewSalek, Sam / Mallia-Milanes, Andrea / McAuslane, Neil / Walker, Stuart et al. | 2012
- 84
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CPI™ Certification as Predictor of Clinical Investigators’ Regulatory ComplianceVulcano, David M. et al. | 2012
- 88
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Providing Medical Information for Orphan DrugsTurbeville, Sean / Wells, David A. / Hornfeldt, Carl S. et al. | 2012
- 94
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The Correction of Product Information in Drug References and Medical TextbooksPharmD, Ching Lum / PharmD, Soo Mi Ahn et al. | 2012
- 99
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The Association Between Leukotriene-Modifying Agents and Spontaneously Reported SuicideSchumock, Glen T. / Gibbons, Robert D. / Lee, Todd A. / Joo, Min J. / Stayner, Leslie T. / Valuck, Robert J. et al. | 2012
- 107
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The Role of Pharmaceutical Medical Information in Promotional Review: Three Benchmarking SurveysBonk, Lisa / Kothari, Madhuri / Andrikanich, Alyson Sous / Yang, Ellen et al. | 2012
- 115
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Text Analytics for Surveillance (TAS): An Interactive Environment for Safety Literature ReviewChristensson, Camilla / Gipson, Geoffrey / Thomas, Tracey / Weatherall, James et al. | 2012
- 124
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The Electronic Common Technical Document (eCTD): An International Pro/Con Analysis of the Pharmaceutical Product Electronic Submission ProcessSuchanek, Andreas / Ostermann, Herwig et al. | 2012
- 140
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Cobert’s Manual of Drug Safety and PharmacovigilanceTabor, Edward et al. | 2012