Who Should Attend

• Principal Investigators
• Research Staff and Coordinators
• IRB Chairpersons
• IRB Committee Members
• IRB Administrators and Staff
• Institutional Officials
• Medical Personnel with an interest in human subjects research
• Institution and Agency Legal Counsel
• Patient Advocates

This conference will give participants practical information on conducting biomedical and social behavioral research, provide an update on the regulations and present an overview of the challenges, issues and potential solutions facing the IRB while reviewing and approving research protocols and the investigators when conducting human subject research.