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  1. HHS
  2. OHRP
  3. Education & Outreach
  4. Human Research Protection Training
  5. Human Research Protection Foundational Training
  • About Research Participation
    • Informational Videos
    • Questions to Ask
    • Protecting Research Volunteers
      • Why Have Regulations to Protect Research Participants?
      • What Regulations Protect Research Participants?
      • Who Oversees the Regulations to Protect Research Participants?
      • Is All Human Research Regulated?
      • Who is Responsible for Protecting Research Participants?
    • Additional Resources
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  • Revised Common Rule
  • Human Research Protection Training
    • Human Research Protection Foundational Training
    • Participant-Centered Informed Consent Training
    • Considerations for Reviewing Human Subjects Research
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    • Mini-Tutorials
  • Videos
  • Exploratory Workshop
    • 2024 (Human Research with AI)
    • 2023 (Psychedelics Research)
    • 2022 (Payment for Participation)
    • 2021 (Third-Party Research Risks)
    • 2020 (Single IRB)
    • 2019 (Privacy and Data Research)
    • 2018 (Informed Consent)
  • Luminaries Lecture Series
  • Human Research Protection Program (HRPP) Resources
  • Educational Collaboration with OHRP
    • Research Community Forums (RCFs)
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  • Education & Outreach Archived Materials

Human Research Protection Foundational Training

If your institution would like to incorporate this/ese training(s) on your own learning system for ease of access and tracking, write to OHRP-EDU@hhs.gov.

OHRP offers this comprehensive training on human research protections based on the requirements of the revised Common Rule (or 2018 Requirements). A printable completion certificate is available at the conclusion of each lesson. Note that OHRP does not collect information about who accesses or completes this training.

For NIH-funded human subjects research, investigators and key personnel must fulfill the protection of human subjects education requirement. This can be achieved by completing OHRP’s Human Research Protection Training. Please review NIH’s “Educational Requirement” for additional information.

When HHS Regulations Apply

When HHS Regulations Apply (Lesson 1)
This lesson introduces human research protections, the Common Rule, and the offices and agencies that oversee human subjects research. It takes approximately 35 min to complete.

Click to access a English transcript of this lesson

Click to access a Spanish transcript of this lesson

Go to Lesson 1
What is Human Subjects Research

What is Human Subjects Research (Lesson 2)
This lesson details how the Common Rule regulations define “research” and “human subjects” and explains what it means to be exempt from the Common Rule regulatory requirements. It takes approximately 1 hr and 35 min to complete.

Click to access a English transcript of this lesson

Click to access a Spanish transcript of this lesson

Go to Lesson 2
What are IRBs

What are IRBs (Lesson 3)
This lesson explains the purpose of and membership requirements for Institutional Review Boards, or IRBs. It takes approximately 45 min to complete.

Click to access a English transcript of this lesson

Click to access a Spanish transcript of this lesson

Go to Lesson 3
IRB Review of Research

IRB Review of Research (Lesson 4)
This lesson describes the regulatory requirements for IRB review and the criteria for IRB review and approval under the Common Rule. It takes approximately 1 hr and 40 min to complete.

Click to access a English transcript of this lesson

Click to access a Spanish transcript of this lesson

Go to Lesson 4
Institutional Oversight of Human Research

Institutional Oversight of Human Research (Lesson 5)
This lesson explains the requirements for research institutions and IRBs for ensuring regulatory compliance and oversight of research to protect human participants. It takes approximately 45 min to complete.

Click to access a English transcript of this lesson

Click to access a Spanish transcript of this lesson

Go to Lesson 5
Content created by Office for Human Research Protections (OHRP)
Content last reviewed May 7, 2025
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