Human Subjects Research. GRANTEE shall not conduct non-exempt human-subjects research, as defined by 45 CFR part 46, involving employees of DWS or individuals receiving services (whether direct or contracted) from DWS. Program reporting and evaluation are not considered human-subjects research.
Human Subjects Research. The Contractor shall not conduct research involving human subjects or their private data unless the Contractor obtains prior written approval from the DHS Institutional Review Board (“IRB”) and from any other federal or state agencies whose approval is required for research on human subjects. The Contractor shall fully comply with any requirements imposed by the IRB.
Human Subjects Research. CSU Stanislaus shall follow the campus Policy on the Protection of Human Subjects that governs the protection of the rights and welfare of human subjects in all Sponsored Programs research in which the institution is engaged
Human Subjects Research. This provision is applicable when human subjects research is conducted pursuant to this Agreement. Contractor agrees to comply with USAID policies, to the extent applicable, including without limitation the Common Federal Policy for the Protection of Human Subjects (implemented by USAID at 22 CFR Part 225); the “Procedures for Protection of Human Subjects in Research Supported by USAID”; and the USAID Standard Provision entitled “Protection of the Individual as a Research Subject (APRIL 1998).” The texts of these policies are available on USAID’s website (see below.)
Human Subjects Research. The Contractor may not conduct any research involving human subjects or their private data if the subjects are employees of DHS or individuals receiving services (whether direct or contracted) from DHS, or where DHS has provided funding for a project that includes research in the contract, unless the Contractor has obtained prior written approval from the DHS Institutional Review Board (IRB), and from any other federal or state agencies whose approval is required for research on human subjects. Before conducting such research, the Contractor shall fully comply with any requirements or conditions, including requirements relating to informed consent, imposed by such IRB committees or agencies. DHS Policy Manual, Policy No. 01-10, explains the policies and procedures for obtaining approval from the DHS IRB.
Human Subjects Research. 12.1 Any use of human subjects in the performance of research hereunder shall comply with all applicable laws and government regulations.
Human Subjects Research. This work involves human subjects research. The Caltech Institutional Review Board (IRB) shall be the IRB of record for this project. Caltech IRB approval will be obtained and maintained throughout the term of this project. This work does not involve human subjects research.
Human Subjects Research. The definition of human subject research is that set forth in federal regulations describing humans, research, clinical investigation and other closely related terms promulgated by the Office of Human Subject Protections for Human Subject Research at 45 CFR §46.102, and the Food & Drug Administration regulations of Clinical Investigations at 21 CFR §50.3, §312.3 and §812.3, and as required by California law. Institutional Official – The Institutional Official is the Signatory Official on the Federalwide Assurance (FWA) filed with OHRP to assure compliance with regulations governing protection of human subjects. OHRP requires the Institutional Official to be a high-level official who has authority to represent the institution named in the FWA. Implementing Procedures Procedures to Implement the Reliance Memorandum of Understanding Between Human Research Protection Programs at University of California Campuses, UC Division of Agriculture and Natural Resources, and Xxxxxxxx Berkeley National Laboratory for IRB Review of Multi-Campus Human Subject Research shall be developed and modified as agreed upon by the HRPP directors of the UC Campuses. Each of the UC Campuses agrees to follow these Procedures for human subject research covered by this Reliance MOU. Reliance on another UC IRB The Institutional Officials signing below agree that the HRPP director at his or her campus may elect to accept and rely on the determination of the exemption or the review and approval by the IRB of another. Each of the participating UC Campuses may elect, on a case-by-case basis whether to rely on, or review for another. The Relying Campus remains responsible for assuring compliance with the Reviewing IRB’s determinations and terms of the FWA.
Human Subjects Research. The Recipient cannot draw down funds from the payment system and no obligations may be made against Federal funds for research involving human subjects (as defined by 45 CFR part 46) xxxxx://xxx.xxx.xxx/ohrp/regulations-and-policy/regulations/45-cfr-46/index.html supported by this Agreement for any period not covered by both an Office for Human Research Protections (OHRP) xxxxx://xxx.xxx.xxx/ohrp/register-irbs-and-obtain-fwas/fwas/fwa- protection-of-human-subjecct/index.html approved Federal Wide Assurance and, as required by 45 CFR Part 46 xxxxx://xxx.xxx.xxx/ohrp/register-irbs-and-obtain-fwas/fwas/fwa- protection-of-human-subjecct/index.html, approval from an Institutional Review Board (IRB). This Agreement requires the institution to ensure that all personnel and partners who engage in human subjects research have completed education on the protection of human subjects. Any individual involved in the design or conduct of the study must satisfy this requirement prior to participating in the project. The Recipient bears the ultimate responsibility for safeguarding the rights and welfare of human subjects, as stipulated in 45 CFR Part 46. Failure to comply will result in the immediate suspension and/or termination of this Agreement.
Human Subjects Research. The Contractor may not conduct any research involving human subjects or their private data if the subjects are employees of DHS or individuals receiving services (whether direct or contracted) from DHS, or individuals receiving services funded by DHS, unless the Contractor has obtained prior written approval from the DHS Institutional Review Board (IRB), and from any other federal or state agencies whose approval is required for research on human subjects. Before conducting such research, the Contractor shall fully comply with any requirements or conditions, including requirements relating to informed consent, imposed by such IRB committees or agencies. The Contractor is not entitled to use human subjects information generated in connection with this Contract for any purpose, including scholarly publications or research purposes, unless the Contractor obtained written approval of its research protocol from the DHS IRB prior to the commencement of any research efforts.
