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STANFORD UNIVERSITY Research Consent Form Protocol Title: Investigating Causes of Type 1 Diabetes Protocol Director: Brian J. Feldman, MD, PhD IRB Approval Date: 6/22/2011 IRB Expiration Date: 5/31/2012
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What is sample consent form?
A sample consent form is a standardized document that outlines the terms and conditions of obtaining consent from an individual for a specific purpose.
Who is required to file sample consent form?
The individuals or organizations that require consent from individuals for a particular activity or project are responsible for filing the sample consent form.
How to fill out sample consent form?
To fill out a sample consent form, you need to provide relevant information about the activity or project for which consent is being obtained. This may include details about the purpose, duration, risks, and any rights that the individual may have.
What is the purpose of sample consent form?
The purpose of a sample consent form is to ensure that individuals are fully informed about the activity or project they are consenting to, and to document their voluntary agreement.
What information must be reported on sample consent form?
The sample consent form should include information such as the purpose of the activity, any potential risks or benefits involved, the rights of the individual, and how their personal information will be handled.
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