UHCL Research Regulations and Guidelines
UHCL is required to protect human subjects under its Federalwide Assurance (FWA) for the Protection of Human Subjects with the Department of Health and Human Services (HHS) Office for Human Research Protections (ORHP) and UHCL's policy for the protection of human subjects participating in research programs (Federal and University Guidelines) conducted at or supported by UHCL. The protections apply to studies conducted internally by faculty or staff and to external studies conducted by grantees and contractors. UHCL adheres to the principles outlined in the Nuremberg Code, Belmont Report and the World Medical Association Declaration of Helsinki.
Committee for the Protection of Human Subjects
The Committee for the Protection of Human Subjects (CPHS) is comprised of members from each of the four colleges and includes alternates in case the primary member is not present. Other members include external and non-research individuals. The UHCL CPHS is organized and operated in accordance with the U.S. Code of Federal Regulations and under Federalwide Assurance No. 00004068.
Summary of IRB Project Review Submission Procedures
All necessary forms and directions for submitting an application for review by the CPHS are linked below. The forms open as fillable Word documents. We recommend that you save them to your own hard drive for completion and later submission.
Faculty Sponsors or Principal Investigators
After reviewing the student's CPHS application and documents for accuracy and compliance, please forward all attachments to OSP at firstname.lastname@example.org. OSP will forward applications to one of the college's CPHS representatives for review and approval.
All student researchers are to email completed CPHS application, informed consent form, survey instrument, etc., to their Faculty Sponsor for review of accuracy and compliance.
Forms and Links
(Revised October 2018)
Protocol Submission Checklist - outline of the procedure for submitting a CPHS protocol for review.
Required Training - link to required web-based training for new investigators and study personnel, transfer certification and recertification.
CPHS Application 2019 - Download document, complete and submit to OSP electronically.
Consent and Assent Forms - Provides a number of CPHS-approved template forms, depending on age of participants. Note that the Informed-Informational Research document can be used when CPHS approves the request to waive participant's signature. A request and justification is submitted in the CPHS application, Section 6, "Informed Consent."
PLEASE NOTE: These forms are being provided as SAMPLES ONLY. You should review them carefully to determine if the language is appropriate for your study. You may modify any of these samples, as needed. Please see IRB Consent Form templates for additional information and templates.
Continuing Review Status Request Form - Submit this form along with all updated application materials when renewing your CPHS protocol.
Completed Protocol Review Form - Submit this form if you require documentation of a closed or completed research study.