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Breadcrumb
  1. HHS
  2. OHRP
  3. Education & Outreach
  4. Participating in Human Research and Clinical Trials
  5. Protecting Research Participants
  6. Shared Responsibility
  • 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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  • Upcoming Educational Events
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    • Human Research Protection Foundational Training
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    • Considerations for Reviewing Human Subjects Research
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    • 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

Who is Responsible for Protecting Research Participants?

Printable

Protecting research participants is a responsibility shared by different groups, including:

HHS and OHRP

OHRP

Responsible for the rules that protect volunteers in HHS funded research


FundingOrganizations

Funding Organizations

Ensure that human research is conducted ethically and complies with appropriate rules and standards of protections


ResearchInstitutions

Research Institutions

Agree to comply with the rules and educate research personnel about appropriate conduct toward research volunteers


IRBs

IRBs

Review and oversee research to ensure that research volunteers are adequately protected according to ethical standards and relevant rules


Researchers

Researchers

Carry out scientifically valid and ethical research. Often this includes providing information to help people make an informed decision about participating


Individuals

Individuals

Learn about the risks and benefits associated with a research study through the informed consent process, and make an informed decision about whether to participate


 

Talk to the research team for questions about a research study. OHRP has created a list of Questions to Ask to help participants when meeting with the research team. The institution’s human research protection office and its IRB will address participants’ concerns for the studies it conducts. Find their contact information in the study consent document.

Content created by Office for Human Research Protections (OHRP)
Content last reviewed October 17, 2023
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