Showing results for IRB

FDA-Regulated Research
Addresses U.S. Food and Drug Administration-regulated clinical research and the responsibilities of researchers, IRBs, and sponsors when an FDA-regula...
Recognizing and Reporting Unanticipated Problems Involving Risks to Subjects or Others in Biomedical Research
The U.S. Food and Drug Administration and the U.S. Department of Health and Human Services human subject protection regulations require institutions t...
Research with Subjects with Physical Disabilities & Impairments
Provides an overview of physical disabilities and impairments, and the obligations imposed on IRBs and researchers to ensure that appropriate research...

Why do I have to purchase an additional subscription for my organization?
Your organization’s existing CITI Program subscription allows for users that are affiliated to your organization by way of being an employee, studen...
Students in Research
This module addresses students as researchers and when students are involved in research as participants. It reviews the history and status of key r...
FDA-Regulated Research
Addresses U.S. Food and Drug Administration-regulated clinical research and the responsibilities of researchers, IRBs, and sponsors when an FDA-regula...
Recognizing and Reporting Unanticipated Problems Involving Risks to Subjects or Others in Biomedical Research
The U.S. Food and Drug Administration and the U.S. Department of Health and Human Services human subject protection regulations require institutions t...
Internal Quality Assurance and Quality Improvement of the HRPP
Provides a general overview of how a HRPP quality assurance/quality improvement (QA/QI) audit program may be structured and why, and focuses on two co...
Research Involving Human Subjects (RCR-Refresher)
Provides an overview of the basic ethical principles relating to human subjects research, informed consent process, federal definition of human subjec...
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