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PROTECTION OF HUMAN SUBJECTS USED IN RESEARCHGENERAL GUIDELINES, POLICIES, AND PROCEDURES OF THE TEMPLEUNIVERSITY INSTITUTIONAL REVIEW BOARD SUBCOMMITTEE B FORTH SAFEGUARDING OF THE RIGHTS AND WELFARE
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01
Step 1: Obtain the necessary forms and documents from the Institutional Review Board (IRB) or ethics committee.
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Step 2: Familiarize yourself with the regulations and guidelines for the protection of human subjects in your specific field.
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Step 3: Identify the participants or subjects who will be involved in the study.
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Step 4: Obtain informed consent from the participants, ensuring that they fully understand the purpose and procedures of the study, as well as any potential risks or benefits.
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Step 5: Develop a detailed protocol outlining the study design, procedures, and data collection methods.
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Step 6: Submit the protocol, along with any necessary forms and documents, to the IRB or ethics committee for review and approval.
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Step 7: Implement the study according to the approved protocol, ensuring the safety and well-being of the participants at all times.
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Step 8: Continuously monitor the study and make any necessary adjustments or amendments based on feedback or new information.
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Step 9: Collect and analyze the data obtained from the study in a manner that protects the privacy and confidentiality of the participants.
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Step 10: Report the findings of the study in a clear and transparent manner, adhering to any reporting requirements or guidelines.
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Step 11: Respect the rights and autonomy of the participants throughout the entire research process.
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Step 12: Maintain accurate and detailed records of the study, including documentation of informed consent and any adverse events.

Who needs protection of human subjects?

01
Researchers conducting studies involving human subjects.
02
Scientists and medical professionals conducting clinical trials.
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Academic researchers conducting social science experiments or surveys involving human participants.
04
Healthcare professionals conducting medical research or experiments on human subjects.
05
Pharmaceutical companies conducting drug trials or studies involving human volunteers.
06
Government agencies conducting research involving human subjects.
07
Non-profit organizations conducting research involving human participants.

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Protection of human subjects refers to the ethical guidelines and regulations in place to ensure the safety and rights of individuals participating in research studies or experiments.
Researchers, institutions, and organizations conducting research involving human subjects are required to file protection of human subjects.
Protection of human subjects forms are typically filled out by researchers, following the guidelines provided by the Institutional Review Board (IRB) or Ethics Committee overseeing the study.
The purpose of protection of human subjects is to safeguard the welfare, rights, and privacy of individuals participating in research studies, while ensuring the scientific integrity of the research.
Information such as the study protocol, risks and benefits to participants, informed consent process, data handling procedures, and confidentiality measures must be reported on protection of human subjects forms.
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