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Study Report

To comply with IMR IRB and MRAC requirements you must provide regular reports on any study throughout the study period. Unless otherwise stated a report will be required from the study and signed by at least one Principal Investigator, every 12 months from date of IMR IRB approval.

Steps to Follow

  1. Obtain a copy of the Protocol Reporting Pro Forma.

  2. Complete all sections of the Protocol Reporting Pro Forma.

  3. Submit the completed Protocol Reporting Pro Forma electronically to imrirb@pngimr.pg.org or alternatively by post to:

    IMR Institutional Review Board
    Papua New Guinea Institute of Medical Research
    PO Box 60
    Goroka, EHP 441
    Papua New Guinea

IMR Institutional Review Board

Contact

Dr William Pomat
IRB Secretary

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