About CPHS / IRB review . . .
What requires CPHS review? . . .
Is this "quality improvement" or "research"?
What training is required before I can do any research with humans? . . .
How do I turn my idea into a formal protocol? . . .
Do I need a consent form, and if so, how do I write one? . . .
What is the consent process? . . .
Where can I find templates for consent forms? . . .
How/Where do I submit research for review? . . .
What are fees for IRB review? . . .
A researcher on our team does not have UTHealth LDAP account, but needs access to the research submission in iRIS. How do I set up a Guest Account? . . .
My sponsor is asking for an IRB Registration Letter - where do I get a copy?
How do I contact CPHS? . . .
Where can I get additional research training? . . .
CPHS HELPLINE 713-500-7943iRIS HELPLINE 713-500-7960UTHealth’s Compliance Hotline (1-888-472-9868)
How can we improve this site?
Committee for the Protection of Human Subjects 6410 Fannin, Suite 1100 Houston, Texas 77030 Phone 713.500.7943 Fax 713.500.7951 Email email@example.com
IRIS Support 713.500.7960
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