Institutions' Roles With The CIRB

OVERVIEW

This Quickguide describes Signatory Institutions, Component Institutions, and Affiliate Institutions.
Roles Within CIRB graphic

SIGNATORY INSTITUTION

A Signatory Institution:

  • Has a direct relationship with the CIRB.
  • Signs the Authorization Agreement and the Division of Responsibilities document.
  • Has the option of including Affiliate and Component Institutions.
  • Is responsible for defining the local context considerations and reporting to the CIRB using the Annual Signatory Institution Worksheet.
  • Ensures that all covered entities conform to the local context considerations.

NOTE:  The responsibilities of the Signatory Institution are listed on the Authorization Agreement.  

COMPONENT INSTITUTION

A Component Institution:

  • Operates under a different name than the Signatory Institution.
  • Uses the same Federal-wide Assurance (FWA) number as the Signatory Institution.
  • Adheres to the same local context considerations as the Signatory Institution. Uses the same boilerplate language and institutional requirements of the Signatory Institution.
  • Conducts research that is monitored by the same office as the Signatory Institution.

NOTE: The Signatory Institution has legal authority over the Component Institution.

AFFILIATE INSTITUTION

An Affiliate Institution:

  • Has a direct relationship with the Signatory Institution and its own FWA number.
  • Adheres to the same local context considerations of the Signatory Institution.
  • Uses the same boilerplate language and institutional requirements of the Signatory Institution.
  • Conducts research that is monitored by the same office as the Signatory Institution.

USEFUL TIPS

All institutions where CTEP-sponsored clinical research trials are conducted must have a unique CTEP Site Code.  If you need a CTEP Site Code or have questions, go to the Enterprise Core Unit (ECU) at ecuhelpdesk@mail.nih.gov.

 

 

Updated: May 5, 2020