Fellowship Cinical Trial Education Series for 2013-2014
- Series Syllabus
- Clinical Trial Design (6 slides per page)
- U.S. Drug Development and the Role of the Sponsor (6 slides per page)
- Protocol Development, Review and Approval Process (6 slides per page)
- Statistical Considerations in Trial Design and Data Analysis (6 slides per page)
- Roles of the Research Team (6 slides per page)
- Informed Consent (6 slides per page)
- Documentation and Document Management in Clinical Research (6 slides per page)
- Clinical Data Management (6 slides per page)
- Documenting, Recording, and Reporting of Adverse Events (AEs) and Unanticipated Problems (6 slides per page)
- Clinical Trial Monitoring (6 slides per page)
Overview
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