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Study #1581970 (852) Research Consent Form and Authorization for Use and Release of Individually Identifiable Health Information Collected for ResearchGate: (Page 1 of 12) Subject Name: SSN (last
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Read through the entire form carefully to understand the information being presented.
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Fill in all required personal information accurately, including name, date of birth, and contact details.
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Make sure to provide consent by signing and dating the form at the designated area.
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If there are any sections where you do not understand the information, seek clarification from a medical professional before proceeding.
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Keep a copy of the signed informed consent form for your records.

Who needs main informed consent form?

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Anyone undergoing a medical procedure or treatment that requires consent from the patient or their legal guardian.
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Main informed consent form is a document that outlines 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 that involves human subjects are required to file the main informed consent form.
Main informed consent form should be filled out by providing all necessary information about the study, risks, benefits, and participant responsibilities, in a clear and understandable manner.
The purpose of main informed consent form is to ensure that participants are fully informed about a research study before deciding to participate, and to protect their rights and welfare throughout the study.
Main informed consent form must include details about the study objectives, procedures, risks, benefits, confidentiality, voluntary participation, and contact information for questions or concerns.
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