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Working With Your Institutional Review Board

This article is the seventh in a continuing series focusing on the exemplary attributes of successful research in clinical practice. In a statement published in Journal of Clinical Oncology, ASCO described a core group of standards and exemplary attributes for clinical trial sites.^1–3 The initial article of the series appeared in Journal of Oncology Practice in July 2008. This installment addresses how to work with institutional review boards (IRBs), covering the following elements of the ASCO statement: participation in the clinical trial development process and maintenance of high educational standards.

	Background

 
As noted in the ASCO statement, "first and foremost, . . . [Click for More]

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