Common use of IRB Approval Clause in Contracts

IRB Approval. Tocagen’s principal investigators for the Tocagen Trials shall be responsible for determining whether study information must be submitted to and approved by an appropriate Institutional Review Board (“IRB”), obtaining IRB review and approval if necessary and implementing IRB requirements, if any, relating to informed consent in connection with the performance by Siemens of the Laboratory Services. If an IRB raises any issues concerning the Laboratory Services, Tocagen shall promptly notify Siemens and work with Siemens and Tocagen’s principal investigators to resolve those issues. Tocagen shall submit all IRB approvals applicable to Laboratory Services and related documentation to Siemens for its review and records.