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INSTRUCTIONS FOR AUTHORS ETHICAL GUIDELINE Studies on human subjects must have been approved by the Institutional Review Board (IRB). Also, informed consent must be obtained from the patients who participated in the study. The manuscript must include a statement in the Materials and Methods that informed consent and ethical approval including IRB information has been obtained. These documents can be requested from the editor, reviewer, or publisher. In case of animal study, authors should...

How to fill out studies on human subjects

How to fill out studies on human subjects

1. Determine the research question and objectives.
2. Review ethical requirements and guidelines for human subjects research.
3. Prepare study design, including sampling method and data collection techniques.
4. Obtain necessary approvals from Institutional Review Boards (IRBs) or Ethics Committees.
5. Recruit participants while ensuring informed consent is obtained.
6. Collect data systematically and ensure participant confidentiality.
7. Analyze the data using appropriate statistical methods.
8. Report findings in accordance with ethical standards and regulatory requirements.

Who needs studies on human subjects?

1. Researchers in medicine and health sciences.
2. Pharmaceutical companies developing new drugs.
3. Academic institutions conducting scientific studies.
4. Public health organizations evaluating interventions.
5. Regulatory agencies assessing safety and efficacy of treatments.

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What is studies on human subjects?

Studies on human subjects refer to research involving human participants in order to gain insights into various aspects such as health, behavior, and social sciences.

Who is required to file studies on human subjects?

Researchers and institutions conducting studies that involve human subjects are required to file studies on human subjects, including those affiliated with universities, hospitals, and private companies.

How to fill out studies on human subjects?

To fill out studies on human subjects, researchers should complete the required application forms provided by their Institutional Review Board (IRB), ensuring that they detail the study methodology, participant recruitment, informed consent processes, and potential risks.

What is the purpose of studies on human subjects?

The purpose of studies on human subjects is to gather data that can lead to new medical treatments, improve health outcomes, and increase understanding of human behavior and social conditions.

What information must be reported on studies on human subjects?

Information that must be reported includes the study's objective, methodology, participant demographics, recruitment strategies, consent process, potential risks, and ethical considerations.