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Training Requirements and Resources

Requirements

Training requirements for Investigators and Key Personnel

Resources

Online Tutorials
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NIH (National Institutes of Health)

Educational Presentations
PowerPoint Presentations Protection of Human Subjects in Research Informed Consent Waivers and Alterations IRB Member Orientation IRB Overview: Compliance Issues Single Patient Use of Investigational Drugs
OHRP Educational Videos (YouTube format) Research Use of Human Biological Specimens Reviewing and Reporting Unanticipated Problems and Adverse Events General Informed Consent Requirements IRB Membership Complex Issues with Research Involving Vulnerable Populations IRB Records (1) IRB Records (2)
OHRP Educational Videos (RealPlayer format) Research Use of Human Biological Specimens Reviewing and Reporting Unanticipated Problems and Adverse Events