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Guidelines for Conducting Clinical Research in FMMC : 1. All clinical studies should be reviewed and approved by the IEC BEFORE initiation ofthe study 2.No retrospective approvals will be granted3.Studies

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Ensure compliance with all ethical guidelines and regulations in the research or study.

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Keep a record of the approval from the central institutional ethics committee for future reference.

Who needs central institutional ethics committee?

01

Researchers conducting studies involving human subjects.

02

Institutions or organizations conducting clinical trials or experiments involving human participants.

03

Medical professionals or professionals from related fields engaging in research or data collection involving human subjects.

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Any individual or entity that needs to ensure ethical standards and protection of human rights in their research or study.

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What is central institutional ethics committee?

A central institutional ethics committee is a group established by an organization or institution to review and oversee research involving human participants to ensure ethical standards are met.

Who is required to file central institutional ethics committee?

Researchers and institutions conducting studies that involve human subjects are required to file with the central institutional ethics committee.

How to fill out central institutional ethics committee?

To fill out the central institutional ethics committee application, researchers should provide detailed information about the study design, objectives, participant recruitment, consent procedures, and data handling, adhering to the specific guidelines provided by the committee.

What is the purpose of central institutional ethics committee?

The purpose of the central institutional ethics committee is to protect the rights and welfare of research participants, ensure compliance with ethical standards, and promote integrity in research.

What information must be reported on central institutional ethics committee?

Information that must be reported includes study objectives, methodology, participant information, consent procedures, potential risks and benefits, and how confidentiality will be maintained.

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