IRB/REB definition

IRB/REB means any institutional review board, research ethics board or other similar body or committee that has reviewed the collection and/or conditions of use of Biological Samples and Research Data by Contributor or that is required to review the contribution of Biological Samples and Research Data to SickKids for use in connection with the Program.
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Examples of IRB/REB in a sentence

  • In rare cases, this Implementing Letter would be executed before ethics (IRB/REB) approval or waiver: if that is the case, additional details should be included to outline how ethics approval will be ensured and documented.

  • SPONSOR or designated Consultants shall have an opportunity to review and comment on the Informed Consent form prior to its submission to the IRB/REB for approval.

  • SickKids will not use Biological Samples or Research Data until Contributor has provided a copy of the form of Participant Consent approved by Contributor’s IRB/REB.

  • If the Funders or SickKids elect to terminate funding for the Program, SickKids shall give notice of such termination to Contributor and the Parties shall cooperate to effect the disposition of any unused Biological Samples and any Research Data as is directed by Contributor by written notice given to SickKids within thirty (30) days after such notification of termination is given, and as Contributor warrants is consistent with the terms of the Participant Consents and any applicable IRB/REB approvals.

  • Contributor shall not transfer any Biological Samples or Research Data to SickKids prior to obtaining such IRB/REB approvals, and shall only transfer Biological Samples and Research Data of Participants in respect of for whom a Participant Consent has been signed.

  • INSTITUTION agrees to obtain or cause Principal Investigator to obtain, from each study subject participating in the Clinical Trial, an appropriately signed Informed Consent form in the form required by FDA as approved by the IRB/REB in accordance with 21 C.F.R. Part 50 and the Protocol, and a HIPAA Authorization as required by 45 C.F.R. Part 164.