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INSTITUTIONAL ETHICS COMMITTEE HUMAN RESEARCH (IE CHR) UNIVERSITY COLLEGE OF MEDICAL SCIENCES UNIVERSITY OF DELHI, DELHI 110095 Serial No (IEC Office) Form to be filled by the Principal Investigator

How to fill out institutional ethics committee- human

How to Fill Out Institutional Ethics Committee- Human:

1. Start by gathering all necessary information and documentation relevant to the committee. This may include application forms, protocols, consent forms, research proposals, and any supporting documents.
2. Ensure that you have a clear understanding of the requirements and guidelines set by the institution and any applicable regulatory bodies. Familiarize yourself with the ethical principles and considerations that should be followed when reviewing research involving human participants.
3. Review the documentation and evaluate if the proposed research meets the required ethical standards. This may include assessing the potential risks and benefits to participants, reviewing the informed consent process, and considering the qualifications and credentials of the researchers involved.
4. Complete the necessary forms and provide accurate and concise information. Make sure to address all relevant sections of the application, including the study aims, methodology, participant selection, data management, and any potential conflicts of interest.
5. Append any supporting documents or additional information that may aid the committee in their assessment. This could include relevant literature, previous studies, detailed research protocols, or any other information that may be helpful in understanding the study's ethical implications.
6. Submit the completed application to the appropriate department or individual responsible for reviewing the institutional ethics committee- human submissions. Follow any specific instructions or guidelines provided by the institution regarding submission procedures.
7. Await feedback or notification from the committee regarding their decision. The committee may ask for additional information or clarification before making their final determination.
8. If approved, ensure that the study is conducted in accordance with the approved protocols and ethical guidelines. Continuously monitor and address any ethical concerns that may arise during the course of the research.
9. If the application is rejected, carefully review the committee's feedback and suggestions. Make the necessary revisions and re-submit the application if applicable.

Who Needs Institutional Ethics Committee- Human:

1. Researchers conducting studies involving human participants.
2. Institutions and organizations conducting human research, such as universities, hospitals, research centers, and pharmaceutical companies.
3. Funding agencies that provide financial support for research involving human participants.
4. Academic and professional societies that establish ethical standards and guidelines for research involving human participants.
5. Regulatory bodies and government agencies responsible for overseeing and monitoring research involving human participants.

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What is institutional ethics committee- human?

Institutional ethics committee-human is a committee that reviews and approves research involving human participants to ensure ethical standards are met.

Who is required to file institutional ethics committee- human?

Researchers conducting studies involving human participants are required to file with the institutional ethics committee-human.

How to fill out institutional ethics committee- human?

To fill out the institutional ethics committee-human, researchers must provide detailed information about the study protocol, informed consent process, and measures to protect participants.

What is the purpose of institutional ethics committee- human?

The purpose of the institutional ethics committee-human is to protect the rights and welfare of human participants involved in research studies.

What information must be reported on institutional ethics committee- human?

Researchers must report detailed information about the study protocol, informed consent process, potential risks and benefits, and measures to ensure participant confidentiality.