I just explained data
recording versus
information obtained. Go back and read again if you missed it. If you did read it, then you're too dumb to understand it and should look for a new hobby.
As far as continuing review...none was done and none claimed by the researcher.
The Certificate of Approval will indicate approval of a consent form.
That's all it means. Nothing more. Straight from the WIRB site. Taake note, this is their
policy statement not a
sample clinical trial form which has nothing to do with a
self-report survey study. The consent form was approved before the study and the study was never submitted for review.
We also have links to WIRBs' own process which shows they continue to observe the study.
No, we don't. We have a link to a
sample form for a clinical trial from "Google Docs" and not the WIRB website. You are trying to mislead people by saying this is from the WIRB website. As stated above the Certificate of Approval, by WIRB policy, is the approval of the consent form.
WIRB Statement of Compliance
Western Institutional Review Board (WIRB) is duly constituted, has written procedures for initial and continuing review of clinical trials; prepares written minutes of convened meetings, and retains records pertaining to the review and approval process; all in compliance with requirements of FDA regulations 21 CFR Parts 50 and 56, HHS regulations 45 CFR 46, and International Conference on Harmonization (ICH) E6, Good Clinical Practice (GCP), as applicable. WIRB is registered with OHRP/FDA; our IRB registration number is IRB00000533, parent organization number is IORG0000432 (effective through September 16, 2012).
"Continuing review" is explicitly stated to be for "clinical trials" and clinical trials only. Funny what you see when you view the source and not sample forms from Google docs.