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Dominic.feature Article Informed Consent Process: Overcoming Language Barriers Michael J. Stronger, DDS, MS, OMS NIC Director and Chair, Risk Management Committeeman in October, the OMS NIC Risk Management
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The form informed consent process is a document that explains the risks and benefits of participating in a research study and is signed by the participant to indicate their understanding and agreement.
Researchers conducting a study involving human participants are required to file the form informed consent process.
The form informed consent process is typically filled out by the researcher with detailed information about the study, risks, benefits, confidentiality, and participant rights. The participant then reviews and signs the form.
The purpose of the form informed consent process is to ensure that participants are fully informed about a research study and voluntarily agree to participate.
The form informed consent process must include information about the study purpose, procedures, risks and benefits, confidentiality, voluntary participation, and contact information for questions or concerns.
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