Informed Consent Form. The Central IRB will provide an approved study-wide informed consent form for each Clinical Study included under this Agreement. The form will indicate areas where ABC may add language or otherwise customize the form for its own site. Any modifications will be subject to approval by the Central IRB, which will then provide a final approved consent form to ABC for use at its site.
Appears in 3 contracts
Sources: Institutional Review Board Authorization Agreement, Institutional Review Board Authorization Agreement, Institutional Review Board Authorization Agreement