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IRB USE ONLY Approval Date: November 2, 2012, Expiration Date: June 5, 2013, STANFORD UNIVERSITY Research Consent Form Protocol Director: Darrell Wilson, MD Protocol Title: Type I Diabetes Triplet
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What is intervention consent form?
The intervention consent form is a legal document that is signed by an individual or organization, giving their consent to participate in a specific intervention or program.
Who is required to file intervention consent form?
The individuals or organizations who wish to participate in the intervention or program are required to file the intervention consent form.
How to fill out intervention consent form?
To fill out the intervention consent form, you need to provide your personal details, including your name, contact information, and any relevant information related to the intervention or program.
What is the purpose of intervention consent form?
The purpose of the intervention consent form is to ensure that individuals or organizations fully understand the nature and potential risks associated with the intervention or program, and voluntarily consent to participate.
What information must be reported on intervention consent form?
The intervention consent form typically requires information such as the purpose of the intervention or program, any potential risks or benefits, confidentiality agreements, and the signatures of the participants.
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