Bayla OstrachLesly-Marie BuerBrittany PriceElise HealyKatelyn BenhoffKelly KnudtsonSara Glick2024-11-112024-11-112024-09-19https://hdl.handle.net/1773/52648This document is to help harm reduction programs understand what an Institutional Review Board (IRB) is, what IRBs do, and when to submit a data collection plan to an IRB. We provide an overview of IRBs, explain what it means to collect data from human subjects, discuss the benefits of using an IRB, offer ways to access an IRB, and tell you what to expect when submitting for IRB review.en-USAttribution-NonCommercial 3.0 United Stateshttp://creativecommons.org/licenses/by-nc/3.0/us/Harm reductionSyringe servicesInstitutional Review BoardResearch ethicsTechnical Report