• All the researches requires informed consent from the involved members especially from participants. The researcher must provide or state (evidence or artifact) on the method of consent informing.
  • The objective of the Consent is to ensure the participants or involved parties understand the purpose, procedures of the study, risks, and benefits the research project, the confidentiality terms and conditions, the cost of the study, and compensation.
  • The consent should address the questions/concerns of the participants.

pdfView the official IRB Consent Checklist