Standard Operating Procedures Search Standard Operating Procedures Search Submit Clear Search If you are human, leave this field blank. Add New SOP 101 Policies and Procedures Management View SOP 101 102 Training and Education View SOP 102 103 Management of IRB Personnel View SOP 103 104 IRB Authority and Signatory Authority View SOP 104 105 Non-Federally Funded Research View SOP 105 106 Implementation of the Final Rule View SOP 106 201 Management and Composition of the IRB View SOP 201 202 Duties of IRB Members View SOP 202 301 Research Submission Requirements View SOP 301 302 Administrative Review and Distribution of Materials View SOP 302 303 IRB Review of Submissions View SOP 303 304 IRB Convened Meeting Administration View SOP 304 305 Documentation of IRB Discussions, Decisions and Findings View SOP 305 306 Ad Hoc Consultant Reviewers View SOP 306 307 Expiration of Approval View SOP 307 308 Document Management View SOP 308 401a Non-Human Subjects Research View SOP 401a 401b Research Activities Exempt from IRB Review View SOP 401b 402 Expedited Review View SOP 402 403 Initial Review – Criteria for IRB Approval View SOP 403 404 Continuing Review View SOP 404 405 Review of Amendments to Research Studies View SOP 405 406 Final Project Reports View SOP 406 407 IRB Actions to Approve or Disapprove Research View SOP 407 408 Medical Case Reports View SOP 408 409 Alternative IRB Review Arrangements and Agreements View SOP 409 410 Appeal of IRB Decisions View SOP 410 501 Vulnerable Populations in Research View SOP 501 502 Clinical Research Involving Investigational Drugs and Devices View SOP 502 503 Genetic Research View SOP 503 505 Research Materials in Participants’ Medical Records View SOP 505 506 Emergency Use of a Test Article and Planned Emergency Use View SOP 506 507 Expanded Access View SOP 507 601 Screening, Recruiting, and Advertising for Participant Enrollment View SOP 601 602 Payment for Participation in Research Studies View SOP 602 701 General Requirements of Informed Consent View SOP 701 702 General Requirements of Documentation of Consent View SOP 702 703 Waiver or Alteration of Consent View SOP 703 704 Assent View SOP 704 801 Conflict of Interest View SOP 801 802 Privacy and Confidentiality View SOP 802 803 Research Related Injury View SOP 803 901 Unanticipated Problems Involving Risks to Participants and Others View SOP 901 902 Deviations View SOP 902 903 HRPP and Non-Compliance View SOP 903 904 Administrative Hold, Suspension and Termination of Approved Research View SOP 904 905 Institutional Reporting Procedures View SOP 905 906 Protection of Research Participants View SOP 906 907 Research Complaints and Concerns View SOP 907 908 Routine and For-Cause Audits View SOP 908 909 Institutional Review Board (IRB) Community Outreach View SOP 909
