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St. Luke's University Health Network Informed Consent/Assent Document for Human Subjects ResearchDepartment:Principal Investigator:Telephone:Investigator(s):Telephone:Medical Study Title:Lay Study
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Informed consent document is used to ensure that individuals have all the necessary information before participating in a research study or medical procedure.
Researchers, medical professionals, and institutions conducting research or procedures that involve human subjects are required to file informed consent documents.
Informed consent documents should be filled out by providing thorough information about the study or procedure, risks and benefits involved, privacy protections, and the participant's right to withdraw consent.
The purpose of informed consent document is to protect the rights and welfare of human subjects participating in research studies or medical procedures.
Informed consent documents must include details about the study or procedure, risks and benefits, confidentiality, voluntary participation, and contact information for questions or concerns.
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