IRB definition
Examples of IRB in a sentence
All Studies were and, if still pending, are being conducted in all material respects in accordance with all Applicable Laws, good clinical practices, good laboratory practices, human subject protections, the protocols, procedures and controls designed and approved for such Studies, professional medical and scientific standards, and in accordance with any requirement of an IRB or other Person or board responsible for review of such Studies.
All required approvals and authorizations for clinical trials to proceed have been obtained from an appropriate IRB, and informed consent has been obtained from all subjects enrolled in the studies, in compliance with Applicable Laws.
NCI will not ship Formulary Agent(s) until it receives the Approved Investigator(s)’s IRB Approval Letters, FDA “Study May Proceed” letter, and any revised Protocols responding to the same, as described in the MTA.
INVESTIGATOR shall, where required by Applicable Law, submit the Protocol, informed consent form, written authorization described in Section 5.1(b), and advertising materials used to recruit Study subjects for review and approval to an IRB.
No Study-related procedures under the Protocol may begin until such IRB and Sponsor approval and Subject consent has been obtained.