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)