OHRP definition

OHRP. The Office for Human Research Protections of DHHS.

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OHRP means the Office of Human Research Protections within the U.S. Department of Health and Human Services (DHHS) that is responsible for guidance, compliance, and oversight relative to the DHHS regulations for the protection of human subjects.

OHRP or “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).

Examples of OHRP in a sentence

• General information about Human Subjects Regulations can be obtained through OHRP at ▇▇▇▇://▇▇▇.▇▇▇.▇▇▇/ohrp or (▇▇▇) ▇▇▇-▇▇▇▇.

• While IRB approval is not required at the time of grant award, these grantees will be required, as a condition of award, to provide documentation that an Assurance of Compliance is on file with the Office for Human Research Protections (OHRP).

• Provide documentation that an Assurance of Compliance is on file with the Office for Human Research Protections (OHRP).

• If applicable to Recipient’s program, the Recipient bears ultimate responsibility for protecting human subjects under the award, including human subjects at all sites, and for ensuring that a Federal-wide Assurance (FWA) approved by the Office for Human Research Protections (OHRP) and certification of Institutional Review Board (IRB) review and approval have been obtained before human subjects research can be conducted at each collaborating site.

• This assurance should be submitted to the OHRP in accordance with the appropriate regulations.

• This document must be kept on file by both parties and provided to OHRP upon request.

• The Contractor shall provide written documentation that all human materials obtained as a result of research involving human subjects conducted under this contract, by collaborating sites, or by subcontractors identified under this contract, were obtained with prior approval by the Office for Human Research Protections (OHRP) of an Assurance to comply with the requirements of 45 CFR 46 to protect human research subjects.

• For more information about OHRP, FWA, and IRBs, please see the following link: ▇▇▇▇://▇▇▇.▇▇▇.▇▇▇/ohrp/index.html.

• Research that is approved by the Institutional Review Board (IRB) must meet the Office for Human Research Protections (OHRP) requirements for use of individual client data.

• Such policy need not require, and this Agreement does not require, reporting unanticipated problems, serious or continuing noncompliance, or suspension/termination of such research to OHRP or other agencies when such reporting is not required by the institution’s FWA or policies or otherwise by regulation.

More Definitions of OHRP

OHRP. The Office for Human Research Protections of DHHS. Overall PI: The lead multi-site principal investigator with ultimate responsibility for the conduct and integrity of Research (generally, the initiating principal investigator or funding principal investigator, as applicable).

OHRP. The Office for Human Research Protections of DHHS. Other Party(ies): An Indemnification Participating Institution and its trustees, directors, officers, employees, agents, faculty, students, and IRB members to whom a Responsible Party is responsible and who are eligible to be reimbursed by a Responsible Party Under the Indemnification Addendum.

OHRP means the Office for Human Research Protections, or any successor office, at DHHS.

OHRP means the Office of Human Research Protections within the U.S.

OHRP means the HHS Office of Human Research Protections.