Protection of Human Subjects. The Designated IRB is responsible for adopting and implementing institutional policies and procedures for protecting human subjects with respect to the Research in compliance with its FWA. The Designated IRB is authorized to review, oversee and monitor the Research Site’s compliance with the policies and procedures of the Designated IRB, relevant ethical principles, and applicable state and federal laws, regulations, guidance, and rulings relating to the protection of human subjects (collectively, the “Standards”), with respect to the Research.
Appears in 4 contracts
Samples: Institutional Review Board Authorization Agreement, Institutional Review Board Authorization Agreement, Institutional Review Board Authorization Agreement
