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MODEL CONSENT FOR RESEARCH IN CLINICAL SETTINGSPlace (only) first page on departmental letterhead showing address, telephone, and fax information. INFORMED Conventicle: SPONSOR: PRINCIPAL INVESTIGATOR:
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Model consent for research is a standardized form that outlines the terms of participation in a research study, including risks and benefits, confidentiality, and the rights of the participant.
Researchers conducting studies involving human subjects are required to obtain and file model consent for research.
Model consent for research should be completed by providing all pertinent information about the study, risks, benefits, confidentiality, and participant rights in a clear and understandable manner.
The purpose of model consent for research is to ensure that participants are fully informed about the research study they are being asked to participate in and to obtain their voluntary agreement to take part.
Model consent for research should include information about the study's purpose, procedures, risks, benefits, confidentiality, participant rights, and contact information for questions and concerns.
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