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COMMITTEE FOR ACADEMIC RESEARCH ETHICS Seth GS Medical College & KEM Hospital, Pearl, Mumbai 400 012. Tel: 91 22 2412 2188 / 91 22 2410 7515, email: carecommittee@kem.eduAnnexure 2 AX 02/SOP 07/V3
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How to fill out are institutional review boards

01
Obtain necessary training and certifications in research ethics and human subjects protection.
02
Develop a detailed research protocol that outlines the purpose, methodology, risks, and benefits of the study.
03
Complete the required application forms and submit them to the Institutional Review Board (IRB) for review.
04
Respond to any feedback or questions from the IRB and make any necessary revisions to the protocol.
05
Obtain approval from the IRB before beginning any research activities involving human subjects.

Who needs are institutional review boards?

01
Researchers conducting studies involving human subjects.
02
Institutions and organizations conducting research that involves human participants.
03
Funding agencies that provide grants for research involving human subjects.
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Institutional Review Boards (IRBs) are committees that are responsible for reviewing, approving, and monitoring research studies involving human participants to ensure ethical and legal compliance.
Researchers conducting studies involving human participants are required to submit their research proposals to IRBs for review and approval before beginning their studies.
Researchers need to submit their research protocols, consent forms, and any other relevant documents to the IRB for review. The IRB will assess the risk and benefit of the study to ensure the protection of human participants.
The purpose of IRBs is to protect the rights and welfare of human participants in research studies by ensuring that studies are conducted ethically and in compliance with regulations.
Research protocols, consent forms, participant recruitment materials, and any other relevant documents must be submitted to IRBs for review.
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Relevant keywords

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