CTN Webinar: IRB and Regulatory Documentation скачать в хорошем качестве

CTN Webinar: IRB and Regulatory Documentation

This one-hour webinar, produced by the National Drug Abuse Treatment Clinical Trials Network (CTN) Clinical Coordinating Center for CTN members and the public, is intended to assist CTN affiliated research staff understand the principles that govern human subject research and the importance of informed consent in research trials. The target audience includes CTN members and members of the public interested in learning more about the process, principles, and requirements involved in working with human subjects in clinical trials. Presented by Lynn Kunkel, MS, CCRP (Oregon Health & Science University, WS Node) and Jennifer Sharpe Potter, PhD (University of Texas, TX Node). For more resources related to this webinar, as well as other webinars in this series, visit: http://ctndisseminationlibrary.org/ct...