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IRB NUMBER: 1107513 IRB APPROVAL DATE: 06/05/2018 IRB EXPIRATION DATE: 06/04/2019UNIVERSITY OF CALIFORNIA, SAN FRANCISCO Consents TO PARTICIPATE IN A RESEARCH STUDY Title: FUNCTIONAL ASSESSMENT IN
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Read the consent form thoroughly to understand the purpose of the study and what it entails.
02
Fill in personal information accurately, such as name, age, contact details, etc.
03
Understand the risks and benefits involved in the study and make an informed decision.
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Sign and date the consent form to indicate that you agree to participate in the study voluntarily.

Who needs consent formbiomedical study?

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Any individual who is invited to participate in a biomedical study will need to fill out a consent form. This includes participants of all ages, genders, and backgrounds.
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A consent form in a biomedical study is a document that provides information to participants about the study's purpose, procedures, risks, benefits, and their rights, ensuring that they voluntarily agree to participate.
The principal investigator or the research team conducting the biomedical study is typically required to file the consent form on behalf of the participants.
To fill out a consent form for a biomedical study, participants need to read the document thoroughly, understand the information presented, and sign the form where indicated to indicate their consent.
The purpose of a consent form in a biomedical study is to ensure that participants are fully informed about the study and consent to participate based on an understanding of their rights and responsibilities.
The consent form must include information about the study's objectives, procedures, risks and benefits, confidentiality assurances, the right to withdraw, and contact information for questions.
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