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1.1.1SAFETY GUIDE FOR EXPERIMENTSSituation:CanfrancEstacin, HUE SCA (ESAA)Date:January 2020Version:V.0 (Rev. 5)Index1 SAFETY Organization FOR EXPERIMENTS 7 1.1 THE EXPERIMENT COLLABORATION 7 1.2 PREVENTION
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How to fill out human subjects protection and

01
Start by identifying the purpose of the study and the type of human subjects protection required.
02
Obtain the necessary ethical approval or clearance from the relevant institutional review board or ethics committee.
03
Develop informed consent forms and ensure they provide clear and comprehensive information about the study, the potential risks, benefits, and rights of the participants.
04
Recruit eligible participants and obtain their voluntary informed consent before starting the study.
05
Implement appropriate measures to protect the privacy and confidentiality of the participants' personal information.
06
Design protocols and procedures that minimize potential risks to participants while maximizing the potential benefits of the study.
07
Collect data and ensure its accuracy, integrity, and security throughout the study.
08
Monitor and evaluate the study to assess its progress and impact on the participants.
09
Communicate the findings and outcomes of the study in a transparent and accessible manner.
10
Ensure compliance with relevant regulations, guidelines, and standards throughout the entire process.

Who needs human subjects protection and?

01
Researchers, scientists, and professionals conducting studies involving human participants.
02
Institutions and organizations that sponsor and oversee research involving human subjects.
03
Ethics committees, review boards, and regulatory bodies responsible for evaluating and approving human subjects research.
04
Participants or potential participants in research studies, as their rights and well-being need to be protected.

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Human subjects protection refers to the ethical and legal standards put in place to safeguard the rights and welfare of individuals participating in research studies.
Researchers, institutions, and organizations conducting studies involving human subjects are required to file for human subjects protection.
Filling out human subjects protection forms typically involves providing details about the research protocol, informed consent processes, potential risks, and measures for safeguarding participants' rights.
The primary purpose of human subjects protection is to ensure the ethical treatment of participants, minimize risks, and promote informed consent in research activities.
Information that must be reported includes study title, research objectives, participant recruitment methods, informed consent processes, data privacy measures, and potential risks to participants.
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