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This document outlines a training module designed to educate researchers on the ethical and responsible conduct of research involving human subjects, in compliance with NSF mandates, focusing on human
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How to fill out Training Module: The Ethical Use and Treatment of Human Subjects in Research

01
Gather all necessary materials and resources related to the training module.
02
Read through the introduction to understand the purpose and importance of ethical treatment of human subjects.
03
Complete any pre-assessments or surveys if required.
04
Follow the structured content, which may include text, videos, and case studies.
05
Take detailed notes on key concepts, rules, and guidelines presented in the module.
06
Participate in interactive activities or discussions if provided.
07
Complete any quizzes or evaluations at the end of each section to reinforce learning.
08
Review any additional resources or references suggested in the module.
09
Submit any required documentation or certificates upon successful completion.

Who needs Training Module: The Ethical Use and Treatment of Human Subjects in Research?

01
Researchers who plan to conduct studies involving human subjects.
02
Institutional Review Board (IRB) members who review research proposals.
03
Students or staff engaged in research training programs.
04
Medical professionals involved in clinical trials or patient-oriented research.
05
Anyone seeking to ensure ethical compliance in research practices.
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There are ethical issues in using human tissues in precision medicine including informed consent and confidentiality, optimal utilization, quality of tissues and minimizing bias.
Subjects must not be exposed to any risk that can practicably be avoided without impairing the research design. Individuals who propose to conduct research involving human subjects must be qualified by experience and/or training to safeguard the well-being of the subjects of their research.
These principles include voluntary participation, informed consent, anonymity, confidentiality, potential for harm, and results communication. Scientists and researchers must always adhere to a certain code of conduct when collecting data from others.
The identified ethical principles include: respect for participants, informed consent, specific permission required for audio or video recording, voluntary participation and no coercion, participant right to withdraw, full disclosure of funding sources, no harm to participants, avoidance of undue intrusion, no use of
For NIH-funded human subjects research, investigators and key personnel must fulfill the protection of human subjects education requirement. This can be achieved by completing OHRP's Human Research Protection Training.

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The Training Module: The Ethical Use and Treatment of Human Subjects in Research is an educational program designed to inform researchers about the ethical considerations, regulations, and best practices involved in conducting research that includes human participants.
Anyone conducting research involving human subjects, including principal investigators, research staff, and students involved in research projects, is typically required to complete this training module.
To fill out the training module, participants must complete the required educational components, pass any assessments or quizzes included, and submit their completion certificate to the relevant institutional review board or research ethics committee.
The purpose of the training module is to ensure that researchers understand their ethical obligations to protect human subjects, promote informed consent, and adhere to federal and institutional regulations governing research practices.
Participants must report their knowledge of ethical principles, understanding of legal requirements, completion status of the training module, and any specific policies related to the protection of human subjects in their research activities.
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