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NCI CIRB Protocol: ALLIANCE A021602 Consent Version Number: Update 1 Consent Version Date: 041919 Consent Implementation Date: 051519 Page 1 of 13Informed Consent Study Title for Study Participants:
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To fill out the NCI CIRB Protocol Alliance, follow these steps:
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Review the instructions provided by the NCI CIRB Protocol Alliance.
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The NCI CIRB Protocol Alliance is needed by researchers, investigators, or organizations involved in conducting applicable clinical trials with cancer patients. It is particularly relevant for those who intend to collaborate with the National Cancer Institute (NCI) and utilize the Central Institutional Review Board (CIRB) services. The NCI CIRB Protocol Alliance helps streamline the ethical and regulatory review process for multi-site clinical trials, ensuring compliance and protection of participants' rights and welfare.
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The NCI CIRB Protocol Alliance is a collaborative effort aimed at streamlining the review and approval process for clinical trial protocols under the National Cancer Institute's Cancer Trials Support Unit.
Institutional Review Boards (IRBs) and institutions that conduct clinical trials and seek National Cancer Institute support are required to file with the NCI CIRB Protocol Alliance.
Filling out the NCI CIRB Protocol Alliance involves completing the required forms and submitting necessary documentation related to the clinical trial protocol as specified in the guidelines provided by the NCI.
The purpose of the NCI CIRB Protocol Alliance is to ensure the efficient review and oversight of multi-site cancer clinical trials, enhancing patient safety and promoting high-quality research.
Information that must be reported includes details about the clinical trial protocol, investigator qualifications, patient eligibility criteria, risks and benefits, and data collection methods.
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