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Descriptive Project Title Invitation (IRB # ___)[Please also insert your IRB ID# in the footer starting on p. 2. Your IRB ID# is assigned as soon as you create your protocol, before completing or

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1. Download the TCCS-informed-assent-template from a trusted source.
2. Read through the template carefully to understand the information required.
3. Fill out the relevant fields in the template with accurate information.
4. Make sure to include any additional information or details as required.
5. Review the filled out template to ensure all information is accurate and complete.
6. Sign and date the template to indicate your agreement and understanding of the information provided.

Who needs tccs-informed-assent-template?

1. Researchers conducting studies involving children who are below the legal age of consent.
2. Medical professionals obtaining assent from minors for medical procedures.
3. Organizations working with vulnerable populations who require informed assent.

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What is tccs-informed-assent-template?

The tccs-informed-assent-template is a document used to provide informed consent for participants in certain research or assessment processes, outlining the study's purpose, procedures, and potential risks.

Who is required to file tccs-informed-assent-template?

Researchers and organizations conducting studies that involve human participants are required to file the tccs-informed-assent-template.

How to fill out tccs-informed-assent-template?

To fill out the tccs-informed-assent-template, one must provide detailed information about the study, including its objectives, methods, risks, benefits, and ensure that consent is clearly obtained from participants.

What is the purpose of tccs-informed-assent-template?

The purpose of the tccs-informed-assent-template is to ensure that participants are fully informed about the study they are involved in and to obtain their voluntary agreement to participate.

What information must be reported on tccs-informed-assent-template?

Information that must be reported includes the study's objectives, methods, contact information for the researchers, anticipated risks, potential benefits, and the right of participants to withdraw at any time.