Office of Human Research Protections definition

Office of Human Research Protections. (OHRP) means the HHS office that oversees protection of human subjects from research risks under 45 C.F.R. Part 46 (the Common Rule).
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Office of Human Research Protections means the HHS office that oversees protection of human subjects from research risks under 45 C.F.R. Part 46 (the Common Rule).
Sample 1Sample 2

Examples of Office of Human Research Protections in a sentence

  • For more information about reporting requirements, refer to the U.S. Department of Health and Human Services’ Office of Human Research Protections website at http://www.hhs.gov/ohrp/.

  • A Federalwide Assurance (FWA) is an assurance approved for Federalwide use by the Office of Human Research Protections (OHRP) in accordance with Section 103(a) of the Common Rule (see 38 CFR 16.103(a)).

  • Noncompliance with respect to human research participant protection violates the LSUHSC-Shreveport Federalwide Assurance Registration (FWA) with the Office of Human Research Protections (OHRP).

  • Before an application can be funded, a Human Subjects Assurance must be on filewith the Office of Human Research Protections (OHRP).

  • See UW IRB GUIDANCE Risks of Harm from Standard Care and the draft guidance from the federal Office of Human Research Protections, “Guidance on Disclosing Reasonably Foreseeable Risks in Research Evaluating Standards of Care”; October 20, 2014.Information about pediatric blood volume and frequency of draws that would qualify for expedited review can be found in this reference table on the Seattle Children’s IRB website.Click or tap here to enter text.

  • The Office of Human Research Protections (OHRP) recognizes that any adverse event in a trial is a potentially important occurrence because it may reflect additional risks to subjects.

  • USU has a Federal Wide Assurance with the Office of Human Research Protections that commits USU to comply with federal regulations governing human participants in research and which is required for Department of Health and Human Services-funded research.

  • This Institution follows the Office of Human Research Protections (OHRP) guidance on “Engagement of Institutions in Research” to apply this definition.

  • List all parties, including collaborators and subcontractors, who will be “engaged” in the human subjects research project and their roles .According to the U.S. Office of Human Research Protections (OHRP), an investigator is “engaged” in human subjects research if they are a direct prime grant recipient (even if not collecting data), are obtaining informed consent from study participants, or are interacting directly or indirectly with study participants and/or their identifiable data or biospecimens.

  • Principal Investigator and Institution acknowledge that the conditions for use of the NINDS Materials are governed by the Rutgers University Institution Review Board (IRB) and must be in compliance with the Office of Human Research Protections (OHRP), Department of Health and Human Services (DHHS), regulations for the protection of human subjects found at 45 CFR Part 46.

Related to Office of Human Research Protections

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