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INSTRUCTIONS FOR USING THE INFORMED CONSENT FORM TEMPLATE (Please delete this page for final version of the consent form.) Statements, comments, instructions or samples in red italics or green italics
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How to fill out biomedical research informed consent

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How to fill out biomedical research informed consent

01
Read the informed consent form thoroughly and understand its contents.
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Ask any questions you may have about the study or the informed consent form.
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Provide all requested personal information accurately.
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Sign and date the informed consent form.
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Retain a copy of the signed informed consent form for your records.

Who needs biomedical research informed consent?

01
Participants who are involved in biomedical research studies need to provide informed consent.
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Biomedical research informed consent is a process where individuals are provided with information regarding a research study, including risks and benefits, and must voluntarily agree to participate.
Researchers conducting biomedical research studies are required to obtain and file informed consent from participants.
Biomedical research informed consent forms typically include details about the study, risks and benefits, participant rights, and must be signed by the participant.
The purpose of biomedical research informed consent is to ensure that participants are fully informed about a study before deciding to participate, and to protect their rights.
Biomedical research informed consent must include details about the study, potential risks and benefits, participant rights, confidentiality measures, and contact information for the researchers.
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