Basic iRIS instruction
虹膜的学习提交
Log in to虹膜使用您的Uthealth用户ID和密码。单击屏幕右侧的学习助理链接，然后选择添加新研究。选择IRB应用程序。完成IRB申请。IRB应用程序是一种智能表单，问题将根据您选择的答案出现。完成应用程序后，您将被定向到“提交数据包”屏幕。在此面板中附加适当的文档：
Informed Consent
- Informed Consent
- Any other handouts or material that will be given to participant to assist with the consent process
Review Board Forms
- Memorial Hermann Research Application (if the research involves Memorial Hermann Hospital system data or facilities)
Study Documents
- Protocol
- PI and Co-I CVs (attaching the CVs in the user's profile is preferred. Once it is uploaded in the profile, you will not have to attach the CV for each new submission.
- Case Report Forms (Or data collection forms. Please combine the pages or sections of the data collection form or case report form into one PDF before attaching)
- Recruitment flyers or advertisements
- Investigator brochures (if applicable)
- Correspondence with the FDA (for clinical investigations initiated by a sponsor investigator)
- Letters of approval from other institutions involved in the research (e.g., HISD, Other IRB approvals, etc.)
- Diagnostic Imaging Review and Approval Form (if research involves diagnostic imaging procedures)
- 病理审查和批准表（如果研究涉及病理的标本）beplay苹果手机能用吗
When you have attached all the documents, click Signoff and Submit. You will be directed to a panel that lists names of study personnel. Check the boxes next to the names of all the co-investigators so that the application packet is routed to them for signature and COI disclosure. When everyone has signed off, the application will be sent to the CPHS queue. You may check the status of the application at anytime by checking Workflow Tracking.
Tips for Successful IRB Submission
Detailed: Entering a Protocol in iRIS
CPHS HELPLINE 713-500-7943
Iris热线索林713-500-7960
Uthealth的合规性热线（1-888-472-9868）
保护人类受试者委员会 IRIS Support713-500-7960 |
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CLINICAL TRIALS RESOURCE CENTEROFFICE OF RESEARCHENVIRONMENTAL HEALTH & SAFETY |
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