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History of Human Subjects Protection
The history of human subjects protection begins with the Nuremberg Code, developed for the
Nuremberg Military Tribunal, as standards by which to judge human experimentation
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How to fill out history of human subjects

How to fill out history of human subjects?
01
Begin by collecting all the necessary information about the human subjects involved in your study. This includes their demographic details, medical history, and any relevant personal or social information.
02
Use a standardized form or template to record the history of human subjects. Ensure that the form includes sections for all the required information, such as identifying details, past medical conditions, current medications, and any previous participation in research studies.
03
Start by capturing the basic demographic information of each human subject, including their name, age, gender, and contact details. This will help in establishing their identity and facilitate communication throughout the research process.
04
Move on to recording their medical history, including any pre-existing conditions, past surgeries, allergies, and family medical history. This information is crucial in assessing the subjects' eligibility for the study and understanding any potential risk factors.
05
Ask about the subjects' current medications, including prescription drugs, over-the-counter medications, and any supplements they may be taking. This will help you identify any potential drug interactions or contraindications that may impact their participation in the study.
06
Inquire about the subjects' previous participation in research studies. This includes asking if they have been involved in similar studies or clinical trials in the past, as well as any adverse events or experiences they may have encountered during those studies.
07
It is important to ensure the privacy and confidentiality of the subjects' personal information. Explain to them how the information will be used, stored, and protected throughout the study, and obtain their consent for collecting and using their data.
Who needs history of human subjects?
01
Researchers and scientists conducting studies involving human subjects require a comprehensive history to understand the individuals involved and their relevance to the research objectives.
02
Institutional Review Boards (IRBs) or Ethics Committees responsible for reviewing and approving research protocols also need access to the history of human subjects to ensure the ethical treatment and protection of participants.
03
Regulatory bodies overseeing research studies, such as the Food and Drug Administration (FDA), may also require the history of human subjects to assess the safety, efficacy, and ethical considerations of the research.
In summary, filling out the history of human subjects involves collecting and recording relevant information about the individuals involved in a research study. This information is necessary for researchers, IRBs, and regulatory bodies to ensure ethical practices and appropriate participant selection in studies.
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What is history of human subjects?
History of human subjects is a record of past participation and relevant information regarding individuals who have been involved in research studies.
Who is required to file history of human subjects?
Researchers or institutions conducting research studies involving human subjects are required to file history of human subjects.
How to fill out history of human subjects?
History of human subjects can be filled out by providing detailed information about each individual participant, such as their demographics, medical history, and any adverse events experienced during the study.
What is the purpose of history of human subjects?
The purpose of history of human subjects is to document and track the involvement of individuals in research studies, including any potential risks or adverse effects.
What information must be reported on history of human subjects?
Information such as the participant's name, age, sex, medical history, any medications taken, and any adverse events experienced during the study must be reported on history of human subjects.
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