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ALL INDIA INSTITUTE OF MEDICAL SCIENCES, JODHPURGuidelines/SOP for Industry Sponsored Clinical Trials of Drugs and New Devices Research Section AIIMS, JodhpurPage 1 of 201. Preamble: Clinical trial
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01
Review the guidelines set by the institute ethics committee for human research.
02
Fill out the necessary forms with detailed information about the research including its purpose, methods, risks and benefits.
03
Ensure that the research protocol adheres to ethical standards and guidelines set by regulatory authorities.
04
Submit the completed forms along with any supporting documents to the institute ethics committee for review and approval.
05
Address any feedback or concerns raised by the committee and make necessary revisions to the research protocol before final approval.

Who needs institute ethics committee human?

01
Researchers or research teams conducting studies involving human subjects.
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Institutions or organizations involved in human research who need to comply with ethical standards and guidelines.
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The Institute Ethics Committee for human research is a formal group that ensures ethical standards are maintained in research involving human participants. It evaluates protocols for ethical considerations before granting approval.
Researchers conducting studies involving human participants at an institution are required to file with the Institute Ethics Committee.
To fill out the Institute Ethics Committee form, researchers typically need to provide details such as the study purpose, methodology, participant information, consent processes, and potential ethical issues.
The purpose of the Institute Ethics Committee is to protect the rights and welfare of human research participants, ensuring that all research complies with ethical standards.
Information that must be reported includes study objectives, research design, participant population, informed consent procedures, and any potential risks and benefits.
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