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? . . .
My sponsor is asking for an IRB Registration Letter - where do I get a copy?
Where can I get additional research training? . . .
Please contact the IRB office for answers to questions, express concerns, and convey suggestions regarding human subjects protections.
IRB Office House: Thursdays, 1–4pm via Teams Room
Email: [email protected]
IRB Helpline: 713-500-7943 (please leave a message and we will get back to you as soon as possible)
iRIS Helpline: 713-500-7960
IRB Review Feedback: IRB Survey
Houston, Texas 77030
Phone: 713-500-7943
Email: [email protected]
Committee for the Protection of Human Subjects
IRIS Support: 713-500-7960
