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For IIEC meeting (final)DRAFT ICMR GUIDELINES FOR COMMON ETHICS REVIEW OF MULTICENTRE RESEARCH 2019Indian Council of Medical Research1For IIEC meeting (final)TABLE OF CONTENTS Section 1 Section 2
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01
Gather relevant research data and documentation.
02
Review the draft ICMR guidelines thoroughly.
03
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04
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05
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Complete all required forms and sections accurately.
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08
Double-check for compliance with ethical standards.
09
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Who needs draft icmr guidelines for?
01
Researchers conducting studies involving human subjects.
02
Medical professionals seeking guidelines for ethical approval.
03
Institutional review boards reviewing study proposals.
04
Academic institutions involved in medical research.
05
Policy-makers interested in standardizing research protocols.
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What is draft icmr guidelines for?
The draft ICMR guidelines provide a framework for ethical and scientific conduct in medical research involving human participants.
Who is required to file draft icmr guidelines for?
Researchers, institutions conducting clinical trials, and organizations involved in biomedical research are required to file the draft ICMR guidelines.
How to fill out draft icmr guidelines for?
To fill out the draft ICMR guidelines, one must gather necessary documentation, complete the application forms, and submit them to the appropriate ethics committee.
What is the purpose of draft icmr guidelines for?
The purpose of the draft ICMR guidelines is to ensure the protection of participants' rights, safety, and well-being in medical research.
What information must be reported on draft icmr guidelines for?
Researchers must report information related to study design, participant consent, risk assessment, and compliance with ethical standards.
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