Provider: New Immigrant Survey

Condition:
Extras Administration: IRB required

Language from Contract:
I.3 Receiving Institution - The university or research institution employing the Investigator and at which the Investigator will conduct research using restricted data obtained through this agreement. The receiving Institution must have an Institutional Review Board/Human Subjects Review Committee registered with the United States Office for Human Research Protections or the National Institute of Health.

V. A-C The Receiving Institution represents and warrants that:
A. The Receiving Institution has an IRB/Human Subjects Protection Committee in accordance with the DHHS regulations codified at Title 45 Part 46 of the Code of Federal Regulations. Proof of such certification and the Institution's Multiple Project Assurance (MPA) or Federalwide Assurance (FWA) number has been provided to NIS.
B. The Receiving Institution's IRB/Human Subjects Protection Committee has reviewed and approved the Research Plan, the Restricted Data Agreement, and the Restricted Data Protection Plan in accordance with the DHHS regulations codified at Title 45 Part 46 of the Code of Federal Regulations, using the standards and procedures for live human subjects, and that certification of such approval has been provided to NIS.