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Annex 3. INFORMED CONSENT From This document confirms your consent to participate in the research ___by a student of the Faculty of Communication of Vilnius University, the purpose of which is ___
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Read the informed consent form completely and carefully.
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Informed consent forms are typically required for participants in medical research studies, clinical trials, surgical procedures, and other healthcare interventions where the individual's consent is necessary before proceeding.
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Informed consent form is a document that explains the risks, benefits, and responsibilities of participating in a research study or medical procedure.
Researchers, doctors, or medical professionals who are conducting a study or performing a procedure that involves human subjects.
The informed consent form should be filled out by the participant or their legal guardian, with assistance from the researcher or medical professional.
The purpose of an informed consent form is to ensure that participants understand the risks and benefits of participating in a study or medical procedure, and to give their voluntary consent.
The informed consent form should include details about the study or procedure, risks and benefits, confidentiality, voluntary participation, and contact information for questions or concerns.
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