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RESEARCH PARTICIPANT CONSENT FORM CAREER: Actualizing Latent Diversity: Online Qualitative Data Collection PI: Allison Godwin, PhD School of Engineering Education Purdue University Key Information
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Informed consent guidelines refer to a set of rules and procedures that ensure individuals are fully informed before agreeing to participate in a study or medical procedure.
Researchers, doctors, and other individuals conducting studies or medical procedures are required to file informed consent guidelines.
Informed consent guidelines can be filled out by providing detailed information about the study or procedure, risks and benefits, and obtaining the signature of the participant.
The purpose of informed consent guidelines is to protect the rights and welfare of individuals participating in studies or medical procedures.
Information such as study details, risks and benefits, confidentiality, and participant rights must be reported on informed consent guidelines.
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