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