IRB Sample Clauses
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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 ▇▇▇▇▇▇▇ & ▇▇▇▇▇▇ 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 ▇▇▇▇▇▇▇ & ▇▇▇▇▇▇ 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. 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. Due to the nature of this qualitative research study, retrieving IRB approval was necessary. Before Phase 1of the MUSE project was implemented in Kampala, Uganda, data collection activities and protocols were reviewed and approved by Internal Review Boards (IRBs) at Emory University (USA; IRB 00110271), and Makerere University (Uganda; Ref. No. 2019-038). Consenting of each participant took place before each cognitive interview began. Each of the data collectors were trained on the consenting process. All of the consent documents were in English and translated to Luganda if necessary. In the consenting process, each participant was explained what was expected from them. Participants were allowed to skip questions if it made them feel uncomfortable, to ask questions during any point of the cognitive interview, and could stop the interview at any point. Each participant was asked to sign the consent form. If participants could not write, they gave a thumb print as a signature while a note taker was present in order to serve as a witness to the process.
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. 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. 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 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. The board, committee or other group (either Institutional Review Board or Ethics Committee) formally instituted to review and approve the initiation of, and conduct periodic review of research involving human subjects.
IRB. Site will conduct Study with the initial and continuing approval of an IRB.