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LINDA BERLIN, PAY. D. & PSYCHOLOGICAL ASSOCIATES, P.A. CLINICAL PSYCHOLOGY GENERAL PSYCHIATRY CHILD AND ADOLESCENT PSYCHIATRY1725 N. University Dr., Suite 350 7000 West Palmetto Park Rd. Suite 407
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Read the entire informed consent document carefully.
02
Understand the purpose of the study and the potential risks and benefits involved.
03
Seek clarification from the researchers or the university if there is any part of the informed consent that you do not understand.
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Ensure that you meet the eligibility criteria for participating in the study.
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Provide your informed consent by signing the document only if you fully understand and voluntarily agree to participate.
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Keep a copy of the signed informed consent for your records.

Who needs informed consent - university?

01
Anyone who is invited to participate in a research study conducted by a university needs to provide informed consent.
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This includes students, faculty members, staff, or any other individual who meets the study's eligibility criteria.
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Informed consent - university is a legal document detailing the risks and benefits of participating in a research study conducted by a university.
The researchers conducting the study and the participants involved are required to file informed consent - university.
Informed consent - university is filled out by providing detailed information about the research study, risks and benefits, participant rights, and obtaining signatures from the participants.
The purpose of informed consent - university is to ensure that participants are fully informed about the research study they are participating in and voluntarily agree to be part of it.
Information such as study objectives, procedures, risks, benefits, confidentiality, contact information, and participant rights must be reported on informed consent - university.
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