院校检讨委员会
关于IRB
The Mission of the 院校检讨委员会s at the University of Texas 里奥格兰德河谷 is to ensure that all Research participants are treated fairly and ethically and to assist Researchers at 金沙中国 in the inclusion of human subjects protections in both their study designs and implementation. The Research合规办公室 assists the IRB by facilitating Research reviews and providing administrative support. For more information on the Health Affairs IRB, please visit the IRB的支持 page 或电子邮件 the Research合规办公室 at irb@discover-motors.com 或致电(956)665-3598.
IRB/Clinical Research Announcement Templates
- The purpose of the templates is for Researchers to make announcements about participation in studies/recruitment, 演讲者的演讲, 等.
- Choosing to use any of these three templates can expedite the process because they are already pre-approved by 金沙中国 Marketing and the IRB Office. You still need IRB approval for the content of the flyers, but the IRB already approves of the overall look.
- Choosing to use a different template will likely result in a delay of approval for your Research project. Different templates must get approved first by 金沙中国 Marketing and then by the IRB before moving forward.
- If you have any questions, please contact us at 林赛.simon@discover-motors.com.
IRB互惠协议
In order to avoid duplication of IRB applications to two separate review committees when conducting multi-site studies, 15 UT universities have IRB互惠协议. For more information on 德克萨斯大学 System Reciprocity Agreements, please visit 院校检讨委员会 for Human Subjects Research 或电子邮件 irb@discover-motors.com.
Master Agreements for Clinical Trials/Studies
Master agreements are available as starting points for negotiations with Research sponsors for clinical and, 在某些情况下, preclinical or other types of studies. 教师 members are welcome to use these agreements as starting points; however, all contracts must be processed through the appropriate office at each UT Institution. For more information, please visit the Research合规办公室 where you can find the most current list of companies with whom UT System has executed master agreements for clinical trials/studies on behalf of their component institutions. 你也可以发邮件给他们 Researchcompliance@discover-motors.com.
培训
Human Subjects Protection 培训 (CITI)
An active CITI Human Subjects Protection 培训 and Responsible Conduct of Research 培训 is required for all members of the Research team. The Human Subjects Protection Courses are good for 2 years while the Responsible Conduct of Research Courses are good for 4 years.
The course you should complete depends on the type of Research you are going to conduct. All CITI completion reports must be provided upon submission of an IRB request such as a new project or modification to add someone to the project. If you are submitting a continuation request for extension of approval, be sure to check whether your CITI course is still valid. It should be at least 3 months from expiration. For more information, please visit the Research合规办公室 或者发邮件到 Researchcompliance@discover-motors.com.
额外的监督委员会
帮助 Institutional Animal Care and Use Committee (IACUC) applications for Research, teaching, and testing activities involving animals.
iacuc@discover-motors.com
帮助 Institutional Biosafety Committee (IBC) applications for Research involving recombinant or synthetic nucleic acid molecules and biological hazardous materials.
ibc@discover-motors.com