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InstitutionalEthicsCommittee(IEC) Seth. S. MedicalCollegeandK. E.M. Hospital, Pearl,Mumbai400012. Web:www.kem.eduSelectionandResponsibilitiesofSubjectexpertSOP04/V5.1 Effectivefrom1stJuly2018, Validupto30thJune2020 1.
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How to fill out institutional ethics committee iec

01
Gather all relevant information and documents related to the research study.
02
Fill out the application form provided by the Institutional Ethics Committee (IEC).
03
Provide detailed information about the study protocol, objectives, methodology, risks, benefits, and ethical considerations.
04
Attach any supporting documents such as informed consent forms, questionnaires, and any relevant agreements or approvals.
05
Submit the completed application form and supporting documents to the IEC for review and approval.
06
Address any feedback or revisions requested by the IEC before final approval is granted.

Who needs institutional ethics committee iec?

01
Researchers conducting studies involving human subjects.
02
Institutions or organizations that oversee research activities.
03
Individuals or groups responsible for ensuring ethical standards in research.
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The institutional ethics committee (IEC) is a dedicated committee responsible for reviewing and approving research studies involving human participants.
Researchers, institutions, or organizations conducting research studies involving human participants are required to file the institutional ethics committee (IEC) application.
To fill out the institutional ethics committee (IEC) application, researchers must provide detailed information about the research study, the potential risks and benefits to participants, and the informed consent process.
The purpose of the institutional ethics committee (IEC) is to ensure the protection of human participants in research studies by reviewing study protocols, informed consent documents, and monitoring ongoing research activities.
Researchers must report detailed information about the research study, including the study protocol, potential risks and benefits to participants, informed consent documents, and any conflicts of interest.
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