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Study ID: Pro00034041_MOD000011 Date Effective: 12/16/2020Informed Consent to Participate in Research Involving Minimal Risk Pro # 00034041 1. Participation is completely voluntary; 2. The study team

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How to fill out informed consent to participate

01

Read through the informed consent form carefully to understand all requirements and expectations.

02

Provide accurate and honest information when filling out the form.

03

Sign and date the form to indicate your voluntary agreement to participate in the activity or study.

04

Ask any questions or seek clarification on any aspects of the form before signing it.

Who needs informed consent to participate?

01

Any individual who is being asked to participate in a research study, medical treatment, or any activity that may pose risks or require specific actions.

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What is informed consent to participate?

Informed consent to participate is a process where individuals are provided with information regarding a research study or project and voluntarily agree to take part in it.

Who is required to file informed consent to participate?

Researchers conducting a study or project are responsible for obtaining and filing informed consent from participants.

How to fill out informed consent to participate?

Informed consent forms typically include information about the study, risks and benefits, confidentiality, and participant rights. Participants must read and sign the form to indicate their agreement to participate.

What is the purpose of informed consent to participate?

The purpose of informed consent is to ensure that participants are fully informed about the research study or project, including potential risks and benefits, so they can make an informed decision about whether to participate.

What information must be reported on informed consent to participate?

Informed consent forms typically include details about the study procedures, purpose, risks and benefits, confidentiality, and contact information for the researchers.

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