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FOR IRB USE ONLY IRB ID #: 2019120621001 APPROVAL DATE: 01/19/21 RELEASED DATE: 01/21/21 EXPIRATION DATE: 01/18/22INFORMED CONSENT DOCUMENT Project Title: A Phase II Trial of ADIEU 20 in Combination
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Start by reading the entire informed consent document carefully to understand its purpose and requirements.
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Begin by providing your personal information, such as your name, address, and contact details.
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Follow the instructions provided to answer any questions or provide any additional information required.
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Review each section of the document thoroughly and provide your consent or refusal for each specific activity or procedure.
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Anyone who is planning to participate in a research study, clinical trial, experimental project, or any activity that involves potential risks or impacts on human subjects. Informed consent documents ensure that individuals have a comprehensive understanding of the project and its associated risks, benefits, and procedures, allowing them to make an informed decision about their participation.
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The informed consent document project is a written document that informs individuals about the risks and benefits of participating in a research study.
Researchers conducting a study that involves human participants are required to file an informed consent document project.
The informed consent document project should be filled out by providing clear and concise information about the study, risks, benefits, participant rights, and contact information.
The purpose of the informed consent document project is to ensure that participants are fully informed about a research study before deciding to participate.
The informed consent document project must include details about the study, risks, benefits, participant rights, and contact information for questions or concerns.
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