院校覆核委员会

提交IRB提案

澳门线上赌博平台大学 faculty and students conducting research involving human subjects must obtain 院校覆核委员会 approval before gathering data. IRB的设立是为了保护这些权利, 幸福, 以及个人隐私, to assure a favorable climate for the conduct of scientific inquiry, and to protect the interests of the institutions at 澳门线上赌博平台大学.

通过Sitero Mentor提交协议, please follow these instructional links based on your role at the university:

Sitero Mentor登录

成功提交协议的提示

提交成功协议的提示:

We strive to ensure every researcher has a good experience with the IRB. We want your application to be successful from the start and have developed the tips below to assist you in writing and submitting a successful IRB application.

早开始，早提交. 参考下面的时间表和 IRB清单开始吧.
1. Each research team member must electronically sign the protocol before it can be submitted for review.
2. Before review, all protocols require approval from the department/division chair or dean.
All forms and templates can be found below under the IRB形式 header. 请只使用本校提供的表格，以免延误.
所有pi, co - pi和指导教师必须完成合作机构培训计划(CITI) training before the Institutional Review Board will approve any protocol. CITI training should be completed before submitting a protocol for review. CITI Training is valid for three years following successful completion of 要求 modules.
Clearly describe the informed consent (and/or minor assent) process. A copy of the informed consent form (and/or minor assent form) must be included in your submission. 如果无法获得知情同意, clearly document the procedures that will be used to protect human subjects and request a waiver of informed consent (note: approval of an informed consent waiver is rare).
The informed consent form must be written in language that the subject population can easily read, 要避免使用行话或专业语言. It is suggested that the informed consent form should be written at no higher than an 8th-grade reading level and in the second person (e.g. 你，你，你的).
The completed protocol application must include anything being used to gather data from participants, 如:
1. 调查,
2. 问卷调查、
3. 评估,
4. 作业,
5. 面试的问题,
6. 焦点小组问题，
7. 电子安全检查备忘录;
8. 以及其他相关文件
Submissions will be considered incomplete if all documentation is not included in the initial submission, 哪些因素会延误审查进程.
该协议必须包括所有招聘材料，例如:
1. 广告,
2. 传单,
3. 电子邮件邀请,
4. 信邀请,
5. 及其他相关招聘材料
如果你在非州立大学进行研究, permission is 要求 from each site on their letterhead and signed by the site facilitator, 学校校长, 学校负责人, 等. 才会被批准.
在Sitero Mentor中只接受电子提交. All other paper or emailed versions will automatically be returned to PIs to submit electronically.
Student protocols will not be reviewed until the faculty advisor has approved the submission in Sitero Mentor. Advisors will be electronically notified of the submission and are responsible for timely acceptance/denial.
在得到IRB的批准之前不要开始你的研究. 在大多数情况下, an official stamped and approved copy of the informed consent form will be emailed to the PI. The stamped and approved copy of the informed consent form should be the only copy provided to potential subjects and participants.

人体课题研究花旗认证

所有初级调查员(pi), Co-PIs, 教师顾问, and department/approving chairs of PIs planning to conduct studies are 要求 to attain Collaborative Institutional Training Initiative (CITI) certification in Human Subject Research. Certification information is kept on file per compliance regulations and accessed when a protocol is submitted. 认证需要每3年更新一次. A 帮助文件 for registering and enrolling in CITI courses is available through the Center for Teaching, 学习, 及科技(ctlt@marziodangelo.com).

完成花旗认证:

看到完成花旗认证 or 花旗认证更新帮助文件启动.
访问 www.citiprogram.org.
Be sure to save your CITI registration information for future reference.
To complete your certification, click the Main Menu and follow the instructions.
When you complete the course, save your certification for your records.
Your certification information will be accessed automatically by Sitero when you submit a research protocol.

IRB形式

Please use the forms below when submitting your documentation to the Axiom Mentor system.

IRB清单2018
IRB决策图
- The Office for Human Research Protections (OHRP) provides the following graphic aids as a guide for institutional review boards (IRBs), 调查人员, and others who decide if an activity is research involving human subjects that must be reviewed by an IRB under the requirements of the U.S. 卫生署 and Human Services (HHS) regulations at 45 CFR part 46.
申请在研究样本中使用人类受试者 (example; questions must be answered online in Sitero Mentor)
知情同意2022年7月修订
未成年同意模板于2022年7月修订
调查同意模板2022年7月
电气设备安全检查备忘录2022年7月
申请修改表格C 2022年7月
To request an amendment/modification to previously approved protocols, complete this form and upload it to the Amendments tab of Sitero Mentor.