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Bangladesh Journal of Bioethics 2014; 5(1):2035INFORMED CONSENT OF HUMAN SUBJECTS: A REVIEW Mohammad Crashed Islam Assistant Director Bangladesh College of Physicians and Surgeons (BPS) Mohammadi,
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Start by reading the informed consent form thoroughly to understand its contents.
02
Ensure that you have all the necessary information and resources to complete the form accurately.
03
Begin by filling in your personal details such as your name, age, contact information, etc.
04
Provide a clear and concise explanation of the purpose and nature of the study or procedure.
05
Include any potential risks, benefits, or alternatives that the participant should be aware of.
06
Clearly state that participation is voluntary and that the participant has the right to withdraw at any time.
07
Include a section for the participant to indicate their understanding of the information provided.
08
Provide space for the participant to sign and date the form, indicating their informed consent.
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Make sure to provide a copy of the completed form to the participant for their records.
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Finally, ensure that the informed consent form is securely stored as per legal and ethical guidelines.

Who needs informed consent of human?

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Anyone who is conducting research or a study involving human subjects needs informed consent.
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This includes researchers in scientific fields, medical professionals, psychologists, academic institutions, etc.
03
Informed consent is essential to ensure that participants understand the purpose, risks, and benefits of the study.
04
It helps protect the rights and well-being of human participants and is a fundamental ethical requirement in research.
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Informed consent of human is a process by which individuals are informed about the risks and benefits of participating in a research study, and voluntarily agree to participate.
Researchers conducting studies involving human participants are required to obtain and file informed consent.
Informed consent forms should include clear information about the study, risks and benefits, confidentiality, and the participant's rights. Participants should sign the form to indicate their consent.
The purpose of informed consent is to protect the rights and welfare of human participants in research studies by ensuring they are fully informed before agreeing to participate.
Informed consent forms should include information about the study objectives, procedures, risks and benefits, confidentiality, compensation (if any), and contact information for questions or concerns.
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