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 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”).
University of Maryland Baltimore IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • January 24th, 2022 • Maryland
The Officials signing below agree that the Relying Institution may rely on the Reviewing Institution/IRB for review and continuing oversight of its human subjects research as described:
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).
INSTITUTIONAL REVIEW BOARD (IRB) AUTHORIZATION AGREEMENTIrb Authorization Agreement • May 28th, 2022
IRB AUTHORIZATION AGREEMENTIrb Authorization Agreement • February 7th, 2024
IRB Authorization Agreement Implementation Checklist and Documentation ToolIrb Authorization Agreement • May 5th, 2020
This is the preferred selections version. If more flexible terms are needed, download the blank version from the IRB website.
Montana State University Institutional Review Board (IRB) Authorization AgreementIrb Authorization Agreement • March 26th, 2024
The Officials signing below agree that (name of Institution B) may rely on the designated IRB for review and continuing oversight of its human subjects research described below: (check one)
CTTI Advancing the Use of Central IRBs for Multicenter Clinical Trials Template IRB Authorization AgreementIrb Authorization Agreement • June 8th, 2021
This template IAA is the work product of the CTTI Advancing the Use of Central IRBs for Multicenter Clinical Trials project team and an additional 46 experts from the Human Research Protection Program community who came together during a 2-day expert meeting held June 12-13, 2014 in Rockville, MD.
IRB Authorization Agreement between CHOP & DUIrb Authorization Agreement • January 29th, 2022
Please reference OHRP’s Guidance on “Engagement of Institutions in Research” at http://www.hhs.gov/ohrp/humansubjects/assurance/engage.htm to determine if both CHOP and DU are engaged in the research.
Institutional Review Board (IRB)/Independent Ethics Committee (IEC) Authorization AgreementIrb Authorization Agreement • November 15th, 2022
The Officials signing below agree that INSTITUTION B may rely on the designated IRB for review and continuing oversight of its human subjects research described in the specific protocol 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;
DHMH and the BCHDIrb Authorization Agreement • May 28th, 2015
The JHSPH IRB and the Baltimore City Health Department (BCHD) have in place an IRB Authorization Agreement allowing the JHSPH IRB to serve as the IRB of record for collaborative human subjects research using BCHD sites or facilities, or for which BCHD personnel serve a research role. BCHD explains it this way:
Institutional Review Board (IRB) Authorization AgreementIrb Authorization Agreement • June 18th, 2011
The Officials signing below agree that may rely on the designated IRB for review and continuing oversight of its human subjects research described below: (check one)
Institutional Review Board (IRB) Authorization AgreementIrb Authorization Agreement • October 6th, 2021
The Officials signing below agree that (Institution B) may rely on the designated IRB for review and continuing oversight of its human subjects research described below:
Institutional Review Board (IRB) Authorization AgreementIrb Authorization Agreement • December 8th, 2008
The Officials signing below agree that City of El Paso Fire Department may rely on the TTUHSC IRB for review and continuing oversight of its human subjects research described below: (check one)
Reliance Agreements with IRBs of Other Institutions Updated March 13, 2022Irb Authorization Agreement • February 21st, 2022
There are situations when Clark University researchers are involved in multi-site research or collaborative projects with investigators at other institutions. An IRB Authorization Agreement (IAA) is a special agreement between two institutions that are engaged in human subjects research to establish a Single IRB (or sIRB) with review authority. An IAA allows an institution with a Federalwide Assurance (FWA) to extend the applicability of its FWA to cover investigators at another institution. In practice, this means an institution’s IRB will be the IRB of Record which reviews the study. These agreements help to minimize regulatory burden on the IRB review and approval process by limiting the IRB review to one institution. When signing the IAA, one institution is designated the lead IRB or sIRB of Record. The IRB that relies on the review and oversight of another IRB is said to be “ceding” or delegating oversight to the lead IRB or sIRB.
Institutional Review Board (IRB)/Independent Ethics Committee (IEC) Authorization AgreementIrb Authorization Agreement • July 26th, 2011
This agreement applies to all human subjects research covered by Institution B’s FWA. This agreement is limited to the following specific protocol(s):
Institutional Review Board (IRB)/Independent Ethics Committee (IEC) Authorization AgreementIrb Authorization Agreement • April 11th, 2014
The Officials signing below agree that (Name of Organization)__________________ may rely on the designated IRB for review and continuing oversight of its human subjects described below: (check one)
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.
ContractIrb Authorization Agreement • March 4th, 2005
Department: UAMS Human Research Advisory Committee Policy Number: 2.3 Section: Relationships Effective Date: July 31, 2002 Revision Dates: February 8, 2005; March 5, 2004; November 18, 2002
ContractIrb Authorization Agreement • May 11th, 2016
RE: Agreement to Rely on External IRB External Organization: [EXTERNAL_ORG] Study #: [IRB_ID]Irb Authorization Agreement • September 7th, 2016
This confirms that an IRB Authorization Agreement with the organization identified above has been executed to rely on their IRB for continuing oversight of this study. This agreement specifies the roles and responsibilities of the respective entities.
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)
Institutional Review Board (IRB)/Independent Ethics Committee (IEC) Authorization AgreementIrb Authorization Agreement • July 17th, 2019
The Officials signing below agree that The University of Alabama may rely on the designated IRB for review and continuing oversight of its human subjects research described below: (check one)
Agreements Pg. 1 of 1 Doc Name:IRB Authorization Agreement Rev: [1]Irb Authorization Agreement • December 21st, 2015
Institutional Review Board (IRB) Authorization AgreementIrb Authorization Agreement • February 18th, 2011
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
COMMITTEE FOR THE PROTECTION OF HUMAN SUBJECTS RESEARCH COMPLIANCE SERVICES IRB Authorization Agreement Request FormIrb Authorization Agreement • October 20th, 2015
Purpose: This form is designed to help facilitate the execution of Institutional Review Board (IRB) Authorization Agreements (IAA). An IAA is an agreement between institutions whereby one institution relies on another institution for IRB review.
Agreements Pg. 1 of 1 Doc Name:IRB Authorization Agreement Rev: [2]Irb Authorization Agreement • November 17th, 2017
IRB AUTHORIZATION REQUEST Version 11.01.13.Irb Authorization Agreement • February 20th, 2013
only one institution's IRB will review the study to avoid the need for dual review - either the University at Albany or the collaborating institution.
Institutional Review Board (IRB)/Independent Ethics Committee (IEC) Authorization AgreementIrb Authorization Agreement • November 29th, 2020
The Officials signing below agree that (Name of Institution B) may rely on the designated IRB for review and continuing oversight of its human subjects research described below: (check one)
Institutional Review Board (IRB) Authorization AgreementIrb Authorization Agreement • October 25th, 2021
The Officials signing below agree that __________(name of Institution B) may rely on the designated IRB for review and continuing oversight of its human subjects research described below: ( check one ):
