Institutional Review Board: Standard Operating Procedures

 

The following procedures are utilized by the the IRB and the Research Compliance Office when reviewing submissions for the use of human subjects in research.

 

 

SOP 101.2 IRB Member Responsibilities and Appointment

SOP 201.2 Human Subjects Research Determination

SOP 202.2 Research Intake

SOP 203.2 Exempt Review

SOP 204.2 Expedited Review

SOP 205.2 Full Board Review

SOP 206.2 Continuing Review

SOP 207.2 Modifications

SOP 208.1 Training Requirements for Human Subject Research Personnel

SOP 209.2 Cooperative Research

SOP 210.1 Deception in Research

SOP 211.1 Principal Investigator Responsibilities

SOP 213.1 Multimedia Recording of Human Subjects

SOP 214.1 Recruitment of Research Participants

SOP 212.1 Research with Minors

SOP 216.1 Faculty Research Involving Their Own Students

SOP 304.1 Research Involving Prisoners

SOP 301.1 Unanticipated Problems and Adverse Events

SOP 302.1 Non-Compliance

SOP 303.1 Suspension and Termination

SOP 217.1 Privacy Board and HIPAA Waiver

SOP 401.1 IRB Routine Post-Approval Monitoring

SOP 402.1 IRB For-Cause Post Approval Monitoring (PAM)

 

Related Information

Human Subjects Research IRB Application Process Human Subjects Training IRB Forms and Templates IRB Membership and Meetings Collaborative Research

Contact Us

110 Cordelia Camp
69 East University Way
Cullowhee, NC 28723
828.227.7212