I Peace has obtained approval from an independent Institutional Review Board (IRB) for the process of generating iPSCs—including donor recruiting, screening, blood draw, iPSC generation, storage, and distribution—for commercial use.
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The IRB which reviewed I Peace's process is an Association for the Accreditation of Human Research Protection Programs (AAHRPP) and ISO 9001:2015 accredited IRB that is routinely inspected by the US Food and Drug Administration (FDA) and found to be in good standing and compliant with federal regulations. In accordance with FDA regulations, an IRB is a group that has the authority to approve, require modifications (to secure approval), or disapprove study protocols, informed consent forms, and other related documents. This group review serves an important role in the protection of the rights and welfare of human research subjects, according to the FDA.