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ALL INDIA INSTITUTE OF MEDICAL SCIENCES, BIBINAGAR, Hyderabad Metropolitan Region, TELANGANA 508126 , , , 508126Standard Operating Procedure (SOP) For Institutional Ethics CommitteeInstitutional Ethices
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How to fill out institutional ethics committee aiims

01
Obtain the official application form for the Institutional Ethics Committee (IEC) at AIIMS.
02
Fill out the form completely and accurately, providing all required information about the research study or project.
03
Include detailed information about the study design, objectives, methodology, and potential risks and benefits for participants.
04
Provide any supporting documents, such as research protocols, informed consent forms, and recruitment materials.
05
Submit the completed application form and supporting documents to the IEC at AIIMS for review and approval.

Who needs institutional ethics committee aiims?

01
Researchers conducting medical or healthcare-related studies at AIIMS.
02
Students or faculty members involved in research projects at AIIMS.
03
Any individual or organization that wants to ensure their research study follows ethical guidelines and standards.
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The Institutional Ethics Committee at AIIMS (All India Institute of Medical Sciences) is a body that reviews research proposals to ensure that they are ethically conducted, protecting the rights and welfare of participants.
Researchers and investigators involved in human subjects research at AIIMS are required to file their studies with the Institutional Ethics Committee.
To fill out the Institutional Ethics Committee application, researchers must complete the designated application form, providing details about the study design, participant recruitment, informed consent process, and risk analysis.
The purpose of the Institutional Ethics Committee at AIIMS is to ensure ethical standards in research, promote respect for participants, safeguard their rights, and oversee the ethical implications of research studies.
Researchers must report detailed information such as the study title, objectives, methodology, risks, benefits, participant inclusion/exclusion criteria, informed consent process, and data handling procedures.
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