Institutional Review Board (IRB) Authorization AgreementIrb) Authorization Agreement • January 13th, 2022
This Agreement is to set forth the respective authorities, roles, and responsibilities of each party when a Ceded Review is accepted by the Designated IRB Institution in accordance with the process set forth herein. For purposes of this Agreement, “Research” means any non-exempt human subjects research within the meaning of the Federal Policy for the Protection of Human Subjects or within the meaning of any other federal human subject research regulations or policies. As used in this Agreement, Research may reference a specific study or protocol in which there will be a UM and relying party operating pursuant to the terms of this Agreement, or collectively the studies subject to Ceded Review under this Agreement.
IRB Authorization Agreement Reviewing: Exempt ReviewIrb Authorization Agreement • December 24th, 2020
This Agreement is entered into by and between the institutions identified below (each a “party” and collectively the “parties”).
IRB Authorization AgreementIrb Authorization Agreement • August 11th, 2022
This Institutional Review Board (IRB) authorization agreement is intended to document a formal agreement between the Centers for Disease Control and Prevention (CDC) and an institution that relies on the CDC IRB for review of the activities specified below. This agreement is permitted by the Food and Drug Administration (FDA) regulations governing the protection of human subjects, IRBs, and the conduct of clinical investigations at 21 CFR parts 50, 56, and 312.
IRB Authorization Agreement (IAA) Information & ProceduresIrb Authorization Agreement • February 26th, 2024
It is a written document that provides a mechanism for an institution engaged in research to delegate institutional review board (IRB) review to another IRB.
IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • April 7th, 2021
Salus IRB is registered with the United States Department of Health and Human Services (DHHS) IRB Registration System for OHRP and FDA under parent organization number IORG0005674 and registration numbers IRB00006833 (Board 1), IRB00006834 (Board 2), IRB00009473 (Board 3), and IRB00013027 (Board 4).
IRB Authorization Agreement Request FormIrb Authorization Agreement • October 20th, 2020
Instructions: An IRB Authorization Agreement (IAA) is a mechanism whereby one institution relies on another for IRB review and approval. Submit this form to request an IRB Authorization Agreement in which a Harvard IRB can serve as either the Reviewing or Relying Institution. As the Reviewing Institution, an Institution is responsible for IRB review and continuing oversight. As the Relying Institution, an Institution cedes IRB review and continuing oversight to the Reviewing Institution.
IRB Authorization AgreementIrb Authorization Agreement • August 19th, 2021
Please note: If the FWA lists the Institution A (University of Chicago BSD-IRB), Institution B must remove themselves from the OHRP website when the specific protocol(s) listed below have ended in order to disassociate from Institution A’s FWA.
IRB Authorization AgreementIrb Authorization Agreement • July 16th, 2018
The Officials signing below agree that Institution B may rely on the designated IRB for review and continuing oversight of its human subject research described below: (choose one)
AMENDMENT TO IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • January 15th, 2019
This First Amendment (“Amendment”) is made effective as of the date of last signature below, by and between The University of North Carolina at Chapel Hill (“Reviewing Institution”) and
IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • July 14th, 2022
IRB Authorization Agreement (IAA) Wheaton CollegeIrb Authorization Agreement • May 16th, 2019
The officials signing below agree that __________ (name of Institution B) may rely on the IRB at __________ (name of Institution A) as the designated IRB for review and continuing oversight of its human subjects research described below:
IRB Authorization Agreement – RCI BMT 17-SIBSIrb Authorization Agreement • February 17th, 2024
the Component Institution operates under a different name from the Signatory Institution, but the Signatory Institution has legal authority for the Component Institution;
AMENDMENT TO IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • May 28th, 2021
This First Amendment (“Amendment”) is made effective as of the date of last signature below, by and between The University of North Carolina at Chapel Hill (“Reviewing Institution”) and
IRB Authorization Agreement – External RelianceIrb Authorization Agreement • December 8th, 2017 • Georgia
If GA Tech wishes to rely on another institution, or another institution has requested that Georgia Tech rely on them as the IRB of record, follow the below steps.
IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • May 1st, 2014
This agreement allows The Children’s Hospital of Philadelphia IRB (CHOP IRB) to act as the IRB of record for another FWA Institution.
IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • July 28th, 2017
This agreement allows The Children’s Hospital of Philadelphia IRB (CHOP IRB) to act as the Reviewing IRB for another Institution.
IRB Authorization AgreementIrb Authorization Agreement • May 24th, 2018
Instructions: For processing a request for the WOU IRB to cede review to (rely on) an external IRB, this form would need to be completed by the internal WOU study team. Once the form is completed, it should be submitted as a separate document with the IRB application. Any questions can be forwarded to irb@mail.wou.edu.
IRB Authorization Agreement (For Regis to rely on another IRB for review)Irb Authorization Agreement • July 2nd, 2021
The Officials signing below agree that Reviewing Institution may rely on the Regis University IRB for review and continuing oversight of its human subject research described below.
IRB Authorization Agreement Request – U-M Ceding Oversight to an External IRB ** Complete this form only for projects that require IRB review. U-M does not enter into agreements for Exempt research. Submit an eResearch application for exemption instead.Irb Authorization Agreement • May 5th, 2020
IRB Authorization Agreement Ver 11.01.13Irb Authorization Agreement • February 19th, 2013
Institution A- Name of Institution or Organization Providing IRB Review: University at Albany, State University of New York IRB Registration #: IRB #1 (000000589), IRB#2 (00000590), IRB # 3(00005949) Federalwide Assurance (FWA) #00001970
ContractIrb Authorization Agreement • September 23rd, 2016
Human Research Protections Program (HRPP) IRB Authorization Agreement (IAA) Investigator ChecklistIrb Authorization Agreement • May 10th, 2023
Checklist for researchers in preparing for an IRB Authorization Agreement (IAA) request with a collaborating organization. This process is available for non-Exempt research only. *Please do not submit this checklist with your Application for IRB Authorization Agreement.
IRB Authorization AgreementIrb Authorization Agreement • May 25th, 2018
Instructions: For processing a request for the WOU IRB to serve as the IRB of Record for an external site engaged in research, this form would need to be completed by the WOU internal study team. Once the form is completed, it should be submitted as a separate document with the study application or modification. Please ensure all study information is included for the local and external IRB. Also, the information for the local and external PI should be provided below in the appropriate sections. Any questions can be forwarded to irb@mail.wou.edu.
Human Research Protections Program (HRPP) IRB Authorization Agreement (IAA) Investigator ChecklistIrb Authorization Agreement • March 17th, 2021
Checklist for researchers in preparing for an IRB Authorization Agreement (IAA) request with a collaborating organization. This process is available for non-Exempt research only. *Please do not submit this checklist with your Application for IRB Authorization Agreement.
IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • February 26th, 2024
Perform initial and continuing reviews of submitted research, reviews of amendments; reviews of unanticipated problems that may involve risks to subjects or others; reviews of noncompliance that may represent serious or continuing noncompliance; reviews of local context information provided by Relying Institution/IRB; and reviews of other documents, as needed to be consistent with the applicable federal regulations.
IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • February 19th, 2014
Salus IRB is registered with the United States Department of Health and Human Services (DHHS) IRB Registration System for OHRP and FDA under parent organization number IORG0005674 and registration numbers IRB00006833 (Board 1), IRB00006834 (Board 2), and IRB00009473 (Board 3).
INSTITUTIONAL REVIEW BOARD (IRB) AUTHORIZATION AGREEMENTIrb) Authorization Agreement • June 11th, 2020
This Institutional Review Board (IRB) Authorization Agreement (“Agreement”) establishes the ability for the INSTITUTE/ORGANIZATION IRB to serve as the IRB of record (“IRB of Record”) for research with human subjects conducted at Weill Cornell Medical College (“Research”):
IRB Authorization Agreement (IAA) Information & ProceduresIrb Authorization Agreement • May 15th, 2017
It is a written document that provides a mechanism for an institution engaged in research to delegate institutional review board (IRB) review to an another IRB.
IRB Authorization Agreement – Georgia Tech as IRB of RecordIrb Authorization Agreement • December 8th, 2017 • Georgia
If GA Tech wishes for another institution rely on them, or another institution has requested that Georgia Tech became the IRB of record, follow the below steps:
