Human Subjects Research. CONTRACTOR 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. 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. Conducting human subjects research is advantageous to advance knowledge and ultimately to improve healthcare and health outcomes. The Hospital and University recognize the importance of facilitating human subjects research as part of the joint academic mission. The Hospital and University are also committed to ensuring that human subjects research is conducted in a manner that meets or exceeds ethical standards. The Hospital will operate its own Research Ethics Board (REB) or Boards (or be part of an REB consortium) that will be separate and independent from the University REB and that will be operated in a manner consistent with the principle of harmonization of research ethics and research policies set out in this Agreement. The Hospital agrees its own REB or REBs (or the REB consortium) will adhere to the Tri-Council Policy Statement (and its updates) and applicable legislation, including but not limited to the Personal Health Information Protection Act, 2004 and O.Reg 245/06. In the event that the Hospital does not have its own REB, it agrees to accept the review of a Board accepted by the University. The Hospital and University agree to collaborate, as appropriate and reasonable, in arrangements designed to enhance the effectiveness, efficiency and consistency of ethical review processes.
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. 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. Conducting human subjects research is advantageous to advance knowledge and ultimately to improve healthcare and health outcomes. The Hospital and University recognize the importance of facilitating human subjects research as part of the joint academic mission. The Hospital and University are also committed to ensuring that human subjects research is conducted in a manner that meets or exceeds ethical standards. The Hospital will operate its own Research Ethics Board (REB) or Boards (or be part of an REB consortium or otherwise engage an external REB as a board of record) that will be separate and independent from the University REB and that will be operated in a manner consistent with the principle of harmonization of research ethics and research policies set out in this Agreement. The Hospital agrees its own REB or REBs (or the REB consortium or external REB) will adhere to the Tri-Council Policy Statement (and its updates) and applicable legislation, including but not limited to the Personal Health Information Protection Act, 2004 and O.Reg 245/06. The University and the Hospital will continue to work on harmonization of issues regarding Research Ethics Boards (such as a standardized Human Subjects Research Application form) through the appropriate Toronto Academic Health Science Network Committee. Within the Toronto Academic Health Science Network, human subjects research protocols may undergo full and independent review by several institutional Research Ethics Boards (REBs).
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
3.4.2.1. Detailed procedures for approving and monitoring human subject research can be found on the Office of Research and Sponsored Program’s website under “Research Guidelines,”
3.4.2.2. Research conducted and funded by the Department of Health and Human Services fall under the federal assurance approved by the Office of Human Research Protections.
3.4.2.3. As outlined in the campus policy, the president or designee is authorized to take appropriate action to implement regulations required by funding and regulatory agencies for the protection of human subjects in research.
3.4.2.4. CSU Stanislaus shall maintain one or more Institutional Review Boards to ensure adequate review of proposed research and shall monitor
3.4.2.5. Adequate training of research personnel and for multi- institutional Sponsored Programs engaged in human subjects research shall be guided by the Office of Research and Sponsored Programs.
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. If Grantee conducts human subjects research under this Grant, Grantee accepts full responsibility for safeguarding participants' rights and welfare. Research must follow Xxxxxxx’s policies and all applicable laws, including those on confidentiality, privacy, and data protection, as well as any regulations governing clinical studies. Grantee will actively monitor compliance with these standards throughout the research term.
Human Subjects Research a. Subawardee agrees to conduct human subjects research under this Agreement in compliance with 45 CFR Part 46 and the Standards for Privacy of Individually Identifiable Health Information outlined in the NIH Grants Policy Statement.
b. Subawardee certifies that it has an appropriate OHRP-approved assurance and IRB approval of the research consistent with 45 CFR Part 46 and that it will comply with NIH prior-approval requirements related to the addition of sites not included in the approved application. Subawardee certifies that all key personnel performing Project Activities under this Agreement have received training in the protection of human subjects. 23/29