Abstract：
To protect subjects who participate in human research, Institutional Review Boards (IRBs) play an important role in reviewing research and determining the validity of a study by comprehensively examining it for ethical issues, including invasiveness and management of personal information. They conduct regular and independent reviews to protect the health, rights, and welfare of research subjects. When we as researchers conduct clinical research, we must obtain IRB approval and submit our research for investigation of ethical issues before we begin.
摘要：
为了保护参与人类研究的受试者，机构审查委员会（IRB）在审查研究和通过全面审查研究的伦理问题来确定研究的有效性方面发挥着重要作用，包括侵入性和个人信息的管理。他们进行定期和独立的审查，以保护健康，权利,和研究对象的福利。当我们作为研究人员进行临床研究时，在开始之前，我们必须获得IRB的批准，并提交我们的研究以进行道德问题的调查。
