Fundamental study for Establishing standardized e-Irb Computer system in Healthcare Kim Kwang-Hwan1, Kwon Jeoung A2,4, Kim Dooree3,* 1Dept. of Hospital Management, Konyang University, 158, Gwanjeodong-ro, Seo-gu, Daejeon, 35365, Korea 2Graduate School of Public Health, Yonsei University, Seoul, 03722, Korea 3College of Nursing, Konyang University, 158, Gwanjeodong-ro, Seo-gu, Daejeon, 35365, Korea 4Institute of Health Services Research, Yonsei University College of Medicine, 03722, Korea *Corresponding Author: DooRee Kim. College of Nursing, Konyang University, 158, Gwanjeodong-ro, Seo-gu, Daejeon, 35365, Korea Email: kdr2015@konyang.ac.kr
Online published on 8 August, 2019. Abstract The Ministry of Health and Welfare in Korea has been obliged to establish the IRB. However, in many cases, items that should be included in the review process are omitted in the process of modification. Therefore, this study analyzes the IRB-related deliberations and evaluation forms of the institutional bioethics committee members of public and private universities that were announced for evaluation and certification of the institutional committee in 2016. The data were collected the new review documents and the review exemption documents that are open to the homepage. Then, we analyzed the items included in the paper form for new deliberation and exemption from each university, and analyzed for form standardization of the institutional bioethics committee based on the data. Most of the research proposal and bioethical compliance pledges were included in the new application form, but the manuals for the subjects, the consent form, and the consent form for the use of personal information were often omitted. The e-IRB standardized system should be developed which not only include the form, but also provide information about the contents for protection of research subject and personal information for the researcher or the deliberation committee member. Top Keywords Healthcare, IRB, e-IRB, Bioethics, Standardization. Top |