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