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INSTITUTIONAL ETHICS COMMITTEE (IEC) Seth GS Medical College and KEM Hospital Established in 1986 IEC Preregistration No. ECR/229/last./MH/2013/RR16,IE CII registration No. ECR/417/last./MH/2013 Issued
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01
Determine the submission requirements and deadlines for the institutional ethics committee (IEC) application.
02
Complete the application form with accurate and detailed information regarding the research project.
03
Attach all necessary supporting documents such as research protocols, informed consent forms, and participant recruitment materials.
04
Ensure that all researchers involved in the project have completed appropriate ethics training.
05
Submit the completed application and supporting documents to the designated contact person or committee for review.
06
Respond promptly to any inquiries or requests for additional information from the IEC.
07
Await feedback and approval from the IEC before proceeding with the research project.

Who needs institutional ethics committee iec?

01
Researchers conducting studies involving human participants.
02
Institutions or organizations hosting research projects that involve ethical considerations.
03
Funders or sponsors of research projects that require ethical oversight.
04
Journals or publications requiring proof of ethical approval for publication.
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Institutional Ethics Committee (IEC) is a committee responsible for reviewing and approving research protocols involving human participants to ensure ethical standards are met.
Researchers conducting studies involving human participants are required to file with the Institutional Ethics Committee (IEC).
To fill out the Institutional Ethics Committee (IEC) form, researchers need to provide detailed information about the study protocol, risks and benefits to participants, and how ethical standards will be upheld.
The purpose of the Institutional Ethics Committee (IEC) is to ensure the protection of human participants in research studies and to uphold ethical standards.
The Institutional Ethics Committee (IEC) requires detailed information about the study protocol, informed consent process, risks and benefits to participants, and how confidentiality will be maintained.
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