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Form M0345DUKE UNIVERSITY HEALTH SYSTEMINFORMED CONSENT FORM TO PARTICIPATE IN RESEARCH Individual Patient Exposure and Response in Pediatric Lupus (personal)CONCISE Summary purpose of this research
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How to fill out informed consent form to

01
Read the informed consent form carefully, making sure you understand all the information provided.
02
Fill in your personal information accurately, including full name, date of birth, and contact information.
03
Sign and date the form to indicate that you agree to participate in the activity or study.
04
If applicable, have a witness sign the form as well.
05
Keep a copy of the completed informed consent form for your records.

Who needs informed consent form to?

01
Informed consent forms are typically required for individuals participating in medical studies, clinical trials, research projects, and any other activities that involve potential risks or benefits.
02
Minors (individuals under 18 years old) may require parental or guardian consent in addition to their own consent.
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An informed consent form is a document that informs participants about a study or procedure and ensures that they voluntarily agree to participate after being made aware of the potential risks and benefits.
Researchers or institutions conducting studies involving human subjects are required to file informed consent forms to ensure ethical compliance and protect participants' rights.
To fill out an informed consent form, provide clear and concise information regarding the study, risks, benefits, and participant rights; ensure it is written in understandable language; and obtain the participant's signature to indicate consent.
The purpose of an informed consent form is to protect participants by ensuring they understand what their participation entails and to respect their autonomy in making an informed decision.
The informed consent form must report details about the study's purpose, procedures, risks, benefits, confidentiality, and the right to withdraw at any time without penalty.
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