All Videos

OHRP's Julia Gorey discusses the ways prisoners may become involved in research and trigger subpart C protections, the relevant areas of regulatory concern, and IRB review of subpart C research. (Feb 13, 2017)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

Watch: Prisoner Research 2: Considerations When a Subject Becomes a Prisoner 

OHRP's Jaime Hernandez discusses the structure and roles of IRBs. He presents the regulatory criteria for IRB approval of research to help investigators understand what it takes to submit a successful research protocol. (Presented at the Trinity Health 2016 Virtual Research Summit, Apr 14, 2016.)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

Watch: What You Should Know About IRB Review of Research

Laura Odwazny, from the HHS Office of the General Counsel, addresses how the HHS regulations apply to research using the Internet. Topics include: assessing privacy and identifiability of subject information, using the Internet for recruitment and retention, informed consent, and maintaining confidentiality. (May 8, 2014)

CE: 1:00 CIP Unit (OHRP doesn't provide documentation but viewers can provide the date, time, title, and URL on the CIP recertification application.)

Watch: Conducting Internet Research: Challenges and Strategies for IRBs

The HHS Office of Research Integrity (ORI) and OHRP developed this interactive training video to educate clinical and social researchers on the importance of protecting research subjects and avoiding research misconduct. Viewers assume the role of one of four characters and determine the outcome by making various decisions.

Watch: The Research Clinic

Carol J. Weil, from the National Cancer Institute, and former OHRP staff, Samantha Smith, discuss ethical and regulatory issues involving the collection, storage, and research use of biospecimens including, informed consent frameworks, privacy concerns, the identifiability, models for data sharing, and return of research results. (Nov 20, 2013)

CE: 1:00 CIP Unit (OHRP doesn't provide documentation but viewers can provide the date, time, title, and URL on the CIP recertification application.)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

Watch: Biobanking: When Issues with Tissues Come a’Knockin’

OHRP's Irene Stith-Coleman discusses the requirements and process for registering IRBs and obtaining Federalwide Assurances (FWAs) under the HHS regulations at 45 CFR part 46. This video is for those new to human subjects protection and those seeking to refresh their understanding of the requirements. (Mar 28, 2013)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

Watch: When the Assurance Comes A Knockin': OHRP's FWA and IRB Registration Processes

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)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

Watch: When PIs Come a' Knockin': Everything Investigators Want to Know but are Afraid to Ask

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)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

Watch: When the Feds come a' Knockin': How to Prepare for an OHRP Compliance Evaluation of your Program

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)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

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)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

Watch: IRB Records, part I