IRB. If necessary, the Provider agrees to furnish all documentation concerning Institutional Review Board (“IRB”) reviews, and to submit required documentation to an IRB or Privacy Board should research protocols change. Provider agrees to submit to the LEA any change in waiver status or conditions for approval of the project by an IRB relating to the work described in the research proposal.
IRB. On or prior to the Closing, Holdings shall either (i) cause the Indebtedness under the Loan Agreement dated as of August 1, 1991 between C&A Products (formerly Xxxxxxx & Xxxxxx Corporation) and the Michigan Strategic Fund (the "Loan Agreement") to be completely paid and retired and terminate all obligations under the Loan Agreement and the Reimbursement Agreement dated as of August 1, 1991 between C&A Products (formerly Xxxxxxx & Xxxxxx Corporation and NBD Bank, N.A.) (the "Reimbursement Agreement") or (ii) obtain amendments to or waivers of any terms of the Reimbursement Agreement, the Loan Agreement and any other Contract relating thereto such that the Reimbursement Agreement, the Loan Agreement and the related Contracts will not in any manner adversely affect the ability of C&A Products to pay dividends on or redeem (other than redemptions solely at the option of C&A Products) the Preferred Stock or adversely affect the ability of Holdings or C&A Products to complete the transactions contemplated by the Transaction Agreements or the Commitment Letters.
IRB. The Group will ensure that the Study begins only after the Group has obtained approval from Institutional Review Board for the Study (the “IRB”).
IRB. The term “IRB” means the leading Institutional Review Board as determined by the GPC’s Institutional Review Board (IRB) Authorization Agreement attached hereto as Exhibit D, as amended from time to time.
IRB. The Conducting Party shall be responsible for obtaining any necessary approvals from institutional review boards (each, an “IRB”) including, where applicable, obtaining approval of all Clinical Trial protocols, informed consents, investigator brochures, subject recruitment materials or plans, authorization of disclosure of confidential subject information, and any alterations to or waivers of the same, prior to commencement of any study. The Conducting Party shall modify the protocol or the informed consent without the prior written agreement of the IRB.
IRB. Licensee shall be responsible for obtaining any necessary approvals from institutional review boards (each, an “IRB”) including, where applicable, obtaining approval of all Clinical Trial protocols, informed consents, investigator brochures, subject recruitment materials or plans, authorization of disclosure of confidential subject information, and any alterations to or waivers of the same, prior to commencement of any study. Licensee shall not modify the protocol or the informed consent without the prior written agreement of the IRB.
IRB. The board, committee or other group (either Institutional Review Board or Ethics Committee) formally instituted and with jurisdiction to review and approve the initiation of the Study, and conduct periodic review of research involving human subjects.
IRB. The Conducting Party shall be responsible for obtaining any necessary approvals from institutional review boards (each, an "IRB") including, where ***CERTAIN INFORMATION HAS BEEN OMITTED AND FILED SEPARATELY WITH THE COMMISSION. CONFIDENTIAL TREATMENT HAS BEEN REQUESTED WITH RESPECT TO THE OMITTED PORTIONS. applicable, obtaining approval of all Clinical Trial protocols, informed consents, investigator brochures, subject recruitment materials or plans, authorization of disclosure of confidential subject information, and any alterations to or waivers of the same, prior to commencement of any study. The Conducting Party shall not modify the protocol or the informed consent without the prior written agreement of the IRB.
IRB. This project did not require IRB approval as it was a Special Studies Project which did not conduct research.
IRB. Institution will conduct the Study in accordance with any conditions imposed by the FDA or the Institutional Review Board (“IRB”) at Institution. If Sponsor’s written instructions are inconsistent with the Protocol, the Protocol approved by the IRB will govern the conduct of the Study.
