Common use of Project Clinical Trials Clause in Contracts

Project Clinical Trials. For any Clinical Trial or non-interventional clinical study included in the Project Plan, the terms and conditions governing that component of the Project Plan shall be governed to the maximum extent possible under this Agreement, and the specifics of such work shall be as set forth in the Project Plan, and in any applicable protocol, IND, and IRB approval. The Parties agree that such Clinical Trial will be performed in compliance with all applicable laws and regulations. AMC will sponsor any such Clinical Trials and any non-interventional clinical studies, meaning the AMC will be responsible for filing the IND and obtaining appropriate IRB approvals. For each such AMC-sponsored Clinical Trial, the terms of this Agreement will be supplemented by an IIR Agreement in the form set out in Exhibit B and such other special and supplemental terms as the Parties determine are necessary and appropriate at that time.

Project Clinical Trials. For any Clinical Trial or non-interventional clinical study included in the Project Plan, the terms and conditions governing that component of the Project Plan shall be governed to the maximum extent possible under this Agreement, and the specifics of such work shall be as set forth in the Project Plan, and in any applicable protocol, IND, and IRB approval. The Parties agree that such Clinical Trial will be performed in compliance with all applicable laws and regulations. AMC will sponsor any such Clinical Trials and any non-interventional clinical studies, meaning the AMC will be responsible for filing the IND and obtaining appropriate IRB approvals. For each such AMC-sponsored Clinical Trial, the terms of this Agreement will be supplemented supplemented, if applicable, by an IIR Agreement in the form set out in Exhibit B and such other special and supplemental terms as the Parties determine are necessary and appropriate at that time.time.‌

Project Clinical Trials. For any Clinical Trial or non-interventional clinical study included in the Project Plan, the terms and conditions governing that component of the Project Plan shall be governed to the maximum extent possible under this Agreement, and the specifics of such work shall be as set forth in the Project Plan, and in any applicable protocol, IND, and IRB approval. The Parties agree that such Clinical Trial will be performed in compliance with all applicable laws and regulations. AMC will sponsor any such Clinical Trials and any non-interventional clinical studies, meaning the AMC will be responsible for filing the IND and obtaining appropriate IRB approvals. For each such AMC-sponsored Clinical Trial, the terms of this Agreement will be supplemented by an IIR ESCR Agreement in the form set out in Exhibit B and such other special and supplemental terms as the Parties determine are necessary and appropriate at that time.time.‌