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Understanding the regulations around the secondary use of data and/or specimens can help study teams accurately determine IRB review level and minimize regulatory burden. During her #ACRP2026 session, Leslie Bell with the Medical University of South Carolina (MUSC) will share how a novel IRB review level tool was built to educate investigators, apply regulatory requirements, and guide users through the next steps in developing an IRB application. Add it to your agenda > https://bit.ly/3LzvMVa Ex
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