Common Contracts
4 similar Irb) Authorization Agreement contracts
Institutional Review Board (IRB) Authorization AgreementIrb) Authorization Agreement • January 13th, 2022
This Agreement is to set forth the respective authorities, roles, and responsibilities of each party when a Ceded Review is accepted by the Designated IRB Institution in accordance with the process set forth herein. For purposes of this Agreement, “Research” means any non-exempt human subjects research within the meaning of the Federal Policy for the Protection of Human Subjects or within the meaning of any other federal human subject research regulations or policies. As used in this Agreement, Research may reference a specific study or protocol in which there will be a UM and relying party operating pursuant to the terms of this Agreement, or collectively the studies subject to Ceded Review under this Agreement.
Institutional Review Board (IRB) Authorization AgreementIrb) Authorization Agreement • December 9th, 2020
This Agreement is to set forth the respective authorities, roles, and responsibilities of each party when a Ceded Review is accepted by the Designated IRB Institution in accordance with the process set forth herein. For purposes of this Agreement, “Research” means any non-exempt human subjects research within the meaning of the Federal Policy for the Protection of Human Subjects or within the meaning of any other federal human subject research regulations or policies. As used in this Agreement, Research may reference a specific study or protocol in which there will be a UM and relying party operating pursuant to the terms of this Agreement, or collectively the studies subject to Ceded Review under this Agreement.
Institutional Review Board (IRB) Authorization AgreementIrb) Authorization Agreement • June 17th, 2020
This Agreement is to set forth the respective authorities, roles, and responsibilities of each party when a Ceded Review is accepted by the Designated IRB Institution in accordance with the process set forth herein. For purposes of this Agreement, “Research” means any non-exempt human subjects research within the meaning of the Federal Policy for the Protection of Human Subjects or within the meaning of any other federal human subject research regulations or policies. As used in this Agreement, Research may reference a specific study or protocol in which there will be a UM and relying party operating pursuant to the terms of this Agreement, or collectively the studies subject to Ceded Review under this Agreement.
Institutional Review Board (IRB) Authorization AgreementIrb) Authorization Agreement • June 15th, 2020
This Agreement is to set forth the respective authorities, roles, and responsibilities of each party when a Ceded Review is accepted by the Designated IRB Institution in accordance with the process set forth herein. For purposes of this Agreement, “Research” means any non-exempt human subjects research within the meaning of the Federal Policy for the Protection of Human Subjects or within the meaning of any other federal human subject research regulations or policies. As used in this Agreement, Research may reference a specific study or protocol in which there will be a UM and relying party operating pursuant to the terms of this Agreement, or collectively the studies subject to Ceded Review under this Agreement.
