CharlotteO Ministries adheres to the HHS.gov Institutional Review Board’s (IRB’s) guidelines.
Current IRB Expiration Date: February 18th, 2025
Contact us for IORG# then Search IRB Status
The Compliance Review Procedure in Brief
The Application for Review and Certification of Compliance enables a review of a proposed research study for the purpose of certification of compliance with various governmental and organizational rules and guidelines for the protection of human participants. A critical aspect of compliance is the principal investigator’s described understanding of the present and potential feelings of the proposed research participants and the principal investigator’s plan to ameliorate any possible adverse reaction to participation. Simply, there are inherent risks associated with any research involving interaction with human participants. It is the principal investigator’s responsibility to control to a reasonable extent any potential harm and to have a plan ready to correct any potential harm.
Required Study and Documentation to Conduct Research Concerning Human Participants:
-CharlotteO Ministries’ IRB Handbook
-IRB Guidelines and Information
-IRB Application Portfolio (Exempt, Expedited, or Full Review)
-Use of Approved Editors
-Possible Program Journal Submission
Lead research investigator is Dr. M. Charlotte Oliver, PhD
We do not offer doctoral study IRB certifications. This must be approved through your learning institution. General research proposals may be considered if researcher is not associated with any other institutions that require IRB certification. Standard research outside dissertation study, do not require residency or defense. Upon completion, research study may be considered for submission to our quarterly community journal.
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