All Videos
OHRP staff presentation on investigator obligations when conducting research with human subjects under the HHS regulations. This video is for those new to the field of human subjects research and those seeking to refresh and reinforce their understanding of the regulatory requirements. (Nov 8, 2012)
Watch: When PIs Come a' Knockin': Everything Investigators Want to Know but are Afraid to Ask
Former OHRP staff, Elyse Summers, discusses the history and requirements of the HHS regulations for the protection of human subjects in research. (Jun 7, 2012)
Watch: When the Regs Come a' Knockin': Nuts and Bolts of 45 CFR part 46
Director of OHRP's Division of Compliance Oversight, Kristina Borror, discusses how to respond to allegations of noncompliance and how to prepare for an investigation. (Feb 23, 2012)
In this dramatization, a fictional OHRP presenter ends her presentation and invites questions from the audience. She responds to questions regarding the protections for vulnerable research subjects described in subparts B, C, and D of the HHS regulations at 45 CFR part 46. (Sep 21, 2010)
Watch: Complex Issues with Research Involving Vulnerable Populations
This video shows fictional characters learning about the IRB records requirements described at 45 CFR part 46. The fictional institution hired a consultant to evaluate its human subjects protections program, who made several observations regarding their compliance with the regulations.(Sep 21, 2010)
In this dramatization, the fictional characters meet to review the deficiencies observed in and requirements related to the IRB's meeting minutes and other IRB records. (Sep 21, 2010)
This dramatization starts with a fictional investigator and IRB Chair talking about obtaining legally effective informed consent from potential research subjects. The second scene portrays the investigator obtaining appropriate informed consent from a potential subject. (Aug 24, 2010)
Michael Carome, formerly of OHRP, discusses the criteria for determining if an incident or outcome is an unanticipated problem involving risk to subjects or others (according to the HHS regulations), the differences between adverse events and unanticipated problems, and how to respond . (Jul 5, 2010)
Watch: Reviewing and Reporting Unanticipated Problems and Adverse Events
OHRP's Julie Kaneshiro discusses the challenges and complexities of applying the HHS regulations to activities involving biological specimens and other private information, including when they do and do not apply. This video is best suited for those who already have basic understanding of the HHS regulations. (Jul 5, 2010)
Watch: Research Use of Human Biological Specimens and Other Private Information
In this dramatization, a Signatory Official meets with her staff to discuss establishing an IRB for their institution. The Human Subjects Protections Administrator provides guidance regarding a broad range of topics including IRB membership, quorum requirements, written procedures, and other important information. (Jul 5, 2010)
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