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Ghana Police Hospital (GPH), Institutional Review Board (IRB)

Continuing Review & Study Closure Notification Form

This form is to be used by investigators to request continuing ethical approval for an ongoing study or to formally notify the Ghana Police Hospital Institutional Review Board (IRB) of study completion or early termination.

    GHANA POLICE HOSPITAL (GPH)
    INSTITUTIONAL REVIEW BOARD (IRB)
    CONTINUING REVIEW AND STUDY CLOSURE NOTIFICATION FORM

    SUBMITTER INFORMATION

    Name of Person Submitting Form

    Submitter Email

    SECTION 1: STUDY IDENTIFICATION

    IRB Reference Number

    Title of Study

    Principal Investigator

    Institution / Affiliation

    Original Date of Ethical Approval

    Current Approval Expiry Date

    SECTION 2: TYPE OF SUBMISSION

    Select Submission Type

    [radio* submission-type use_label_element default:1 "Continuing-Review-Renewal" "Study-Closure" "Early-Termination"]

    SECTION 3: PROGRESS REPORT (FOR CONTINUING REVIEW)

    3.1 Summary of Study Progress to Date

    3.2 Number of Participants Approved vs Enrolled

    3.3 Summary of Any Deviations from Approved Protocol

    3.4 Summary of Adverse Events or Unanticipated Problems

    3.5 Assessment of Ongoing Risk-Benefit Balance

    SECTION 5: REQUEST FOR CONTINUED APPROVAL

    Requested Continuation Period

    SECTION 4: AMENDMENTS AND CHANGES

    Have there been any amendments?

    Attach Amendment Details (if applicable)

    SECTION 6: STUDY CLOSURE / TERMINATION REPORT

    6.1 Date of Study Completion or Termination

    6.2 Reason for Early Termination (If Applicable)

    6.3 Confirmation that no further participant contact or data collection will occur

    [radio* participant-contact-confirmation use_label_element "Yes" "No"]

    6.4 Summary of Final Outcomes

    SECTION 7: DATA MANAGEMENT AND FINAL DISPOSITION

    Describe plans for final data storage, confidentiality, and dissemination of results

    SECTION 8: DECLARATION AND SIGNATURE


    I certify that the information provided in this report is accurate and complete. I confirm that the study has been conducted in accordance with the approved protocol and ethical requirements and that the IRB has been notified of study completion or termination where applicable.

    Name of Principal Investigator

    Signature

    Date