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Informed Consent Version 2.4, May 13th, 2020IRB Prot. #74347414 / BZNNFXBMKsInformed Consent Form for Research Involving Human Subjects Protocol Title:New Chemotherapy Regimens and Biomarkers for
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How to fill out informed consent version 2

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Read the informed consent form thoroughly.
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Understand the purpose of the study and risks involved.
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Sign and date the form to indicate your consent.
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Keep a copy of the form for your records.

Who needs informed consent version 2?

01
Participants in research studies or clinical trials.
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Individuals undergoing medical procedures or treatments.
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Patients receiving experimental medications or therapies.
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Informed consent version 2 refers to an updated process or document through which participants in a research study are informed about the study, its procedures, risks, benefits, and their rights before participating.
Researchers and institutions conducting studies involving human participants are required to file informed consent version 2.
To fill out informed consent version 2, researchers must accurately complete the document by providing detailed information about the study, including its purpose, procedures, risks, benefits, and obtaining signatures from participants.
The purpose of informed consent version 2 is to ensure that participants are adequately informed about the research study and voluntarily agree to participate, thereby protecting their autonomy and rights.
Information such as the study's purpose, duration, procedures, potential risks, benefits, confidentiality assurances, and contact information for further inquiries must be reported on informed consent version 2.
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