Showing results for IRB

Mobile Apps and Human Subjects Research
Provides researchers and Institutional Review Boards (IRBs) regulatory information about the use of mobile apps in research. Discusses ethical issues ...
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...
SBE Refresher 1 – Federal Regulations for Protecting Research Subjects
Highlights the topic of IRB regulatory review criteria from the module The Regulations – SBE. Identifies what IRBs must consider to approve research...
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...
Navigating FDA's Updated Informed Consent Guidelines
Introduction The U.S. Food and Drug Administration (FDA) has taken a significant step towards ensuring the protection of human subjects in clinical i...

Are HSR courses eligible for CIP CE education credits?
Yes, advanced-level modules that meet the criteria in the Certified IRB Professional (CIP) recertification guidelines are eligible as accredited conti...
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