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Get the free Informed Consent Form for Parent/Legal Guardian of Minor Participant

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National Cancer Institute / Protocol Number 10323Page 1 of 13Informed Consent Form for Parent/Legal Guardian of Minor Participant Sponsor / Study Title:National Cancer Institute / Cancer Moonshot
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How to fill out informed consent form for

01
Read the informed consent form thoroughly to understand the purpose, procedures, risks, and benefits associated with participating in the activity or study.
02
Complete the demographic information section, providing accurate personal details such as name, age, gender, and contact information.
03
Review the disclosure section carefully, which includes information about any potential conflicts of interest or financial considerations.
04
Understand the terms and conditions of participation, including any obligations, responsibilities, or requirements.
05
Seek clarification from the appropriate authority if you have any questions or concerns regarding the form or its contents.
06
Sign and date the informed consent form to indicate your willingness to participate and acknowledge that you have understood the information provided.
07
Keep a copy of the completed and signed form for your records, if necessary.

Who needs informed consent form for?

01
Informed consent forms are typically required for individuals who are about to participate in activities or studies that involve potential risks or require them to provide personal information or consent.
02
This includes but is not limited to medical and clinical trials, research studies, experimental treatments, participation in surveys or questionnaires, and any situation where informed consent is necessary to ensure ethical considerations and individual autonomy.
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The informed consent form is used to ensure that participants are fully aware of the nature, risks, and benefits of a study or treatment before they agree to participate.
Researchers conducting studies involving human subjects are required to file informed consent forms for their participants.
To fill out the informed consent form, provide accurate information about the study, ensure it is written in clear language, and require participants to read it and sign it voluntarily.
The purpose of the informed consent form is to protect participants' rights and autonomy by informing them about the study they are partaking in and obtaining their voluntary agreement.
The informed consent form must report information about the study's purpose, procedures, potential risks, benefits, confidentiality assurances, and the right to withdraw at any time.
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