Institutional Review Board
Request for In-service
Please complete the contact information:
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First Name
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Last Name
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Work Dept.
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Phone Number
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Email address
The following information will help us plan the in-service:
Approximate # of attendees:
Desired length of presentation:
List several date preferences:
Target Audience:
Faculty
Research Coordinators
Students
Other:
What information would you like for us to present?
Adverse Event Reporting
Advertisements/Recruitment of Subjects
Amendments
Authority of the IRB
Compliance Reviews
Continuing Reviews
Data Safety Monitoring
GRASP Program
History and Ethics leading to the Required Establishment of IRBs
HIPAA and its impact on Research
Important Definitions
IMPACTT
Informed Consent – Process of Obtaining Consent
Informed Consent – Writing an Effective Informed Consent Document
Investigator Responsibilities
IRB Review Processes (e.g., exempt, expedited, full Committee)
Issues Pertaining to Behavioral and Social Science Research
Protocol Deviations
Research Involving Students as Participants
Research Involving Vulnerable Populations – Children
Research Involving Vulnerable Populations – Pregnant Women, Human Fetuses and Neonates
Research Involving Vulnerable Populations – Prisoners
Review of DHHS Regulations
Review of FDA Regulations
Review of the Policies and Procedures of the VU IRB
Waiver of Consent Process and/or Documentation
Please
describe other topics you would like to have presented to your department
: