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INDIANA UNIVERSITY INFORMED CONSENT STATEMENT FORFEITURE RESEARCH USE OF INFORMATION AND BIOSPECIMENS Insert Protocol Title Insert Sponsor Name and Sponsor Protocol Number ABOUT FUTURE Research are
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How to fill out indiana university informed consent

01
Start by reading the informed consent form provided by Indiana University.
02
Make sure you understand the purpose and procedures described in the form.
03
Fill out the required personal information, such as your name, contact details, and any other information requested.
04
Carefully review any risks or benefits associated with participating in the study.
05
If you have any questions or concerns, seek clarification from the appropriate person or contact mentioned in the form.
06
Sign the informed consent form to indicate your voluntary participation and understanding of the study.
07
It is advisable to keep a copy of the filled out informed consent form for your records.

Who needs indiana university informed consent?

01
Anyone who is planning to participate in a study or research conducted by Indiana University will need to fill out the informed consent form. This includes students, faculty members, or any other individual who will be part of the research process.

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Indiana University informed consent is a process used by researchers to inform potential participants about the key elements of a research study before they decide whether or not to participate.
Researchers conducting studies involving human participants at Indiana University are required to file informed consent.
To fill out Indiana University informed consent, researchers must include information about the study purpose, procedures, risks, benefits, confidentiality, and contact information.
The purpose of Indiana University informed consent is to protect the rights and welfare of research participants by ensuring they are fully informed about the study before making a decision to participate.
The information that must be reported on Indiana University informed consent includes the study purpose, procedures, risks, benefits, confidentiality safeguards, contact information, and participant rights.
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