ࡱ> a pbjbjll > Section 4: Participant Information Since the beginning of the research project, please indicate:Total number of subjects who CONSENTED to participateTotal number of subjects who have COMPLETED the studyTotal number of subjects who WITHDREW during the study**If any subjects withdrew from the study, brief explanation of the reason(s) for withdrawal, if known, below.>> Section 5: Summary of Events 1. Did any deviation occur from the protocol submitted since your last IRB approval? AND/OR 2. Did any deviation occur from the originally anticipated risks and/or benefits of the study?If you answered YES to either question, provide a detailed explanation below, including actions taken to reduce the risks or discomforts to subjects and/or to communicate new findings or knowledge to subjects.>> 3. Since the last IRB review, did unanticipated problems, adverse events, or subject complaints occur? If YES, provide a detailed explanation below. Indicate whether you reported the event to the IRB, and if not, explain why.>> Section 6: Data Retention and Storage 1. If you will retain data with direct identifiers or enough indirect identifiers that a participants identity could be determined, indicate the retention/storage plan described in your original protocol.>> 2. [Students only] If you still possess data with identifiers, describe how you will transfer that data to your faculty adviser upon graduation, and 2) describe how he/she will retain the data, and until what point.>> Section 6: Investigator Statement of compliance By submitting this form, I certify that all information provided is accurate and that procedures involved in this project were conducted in strict accordance with federal regulations and ħԴ policies governing human subject research. Signature of Principal Investigator Date (mm/dd/yyyy) Signature of Co-Investigator (if applicable) Date (mm/dd/yyyy) Signature of Co-Investigator (if applicable) Date (mm/dd/yyyy) Signature of Faculty Advisor (if not the PI) Date (mm/dd/yyyy) Important information about retention of informed consent forms and research records: If this study was originally submitted after July 1, 2002, the principal investigator is expected to maintain records of consent as well as the research records for at least three (3) years after the close of the study, unless the study falls under the Health Insurance Portability and Accountability Act (HIPAA). For studies that fall under HIPAA regulation, consent forms and research records must be kept for a minimum of six (6) years. Further guidance on signed informed consent form retention and destruction may be located at  HYPERLINK "http://www.research.psu.edu/orp/areas/humans/samples/retention.asp" http://www.research.psu.edu/orp/areas/humans/samples/retention.asp.     IRB Closeout Report Last Updated: March 2019 SU Institutional Review Board Admin 201, 206-296-2585 irb@seattleu.edu Office Use Only Date Received: IRB Closure Date: mm/dd/yyyy   ./ֿ֯o_N;-h5OJQJ\]aJ$jh5OJQJU\]aJ!h\h^5OJQJ\]aJh^h8Y5CJOJQJaJ h$2hh5CJOJQJaJ h$2h8t5CJOJQJaJ h$2h:5CJOJQJaJ h$2hH;5CJOJQJaJ h^h:5CJOJQJaJ -jh 5CJOJQJUaJ mHnHuh:hQ]5OJQJh]!5OJQJ(jh:hH;OJQJUmHnHu  e  & Fh<P$If^h`gdaW  & Fh<$If^h`gdaW  & Fhd$If^h`gd_xgd;$a$gd; E I N ] b f g ׳ttffWfF!h_xh65OJQJ\]aJh3xh0JOJQJaJjhOJQJUaJhuh5OJQJaJh5OJQJaJhRvh>*OJQJaJhOJQJaJh5OJQJ\]aJ!h\h^5OJQJ\]aJ%hh^0J5OJQJ\]aJ$jh5OJQJU\]aJ*jh5OJQJU\]aJ & B D   8 ? 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