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1RESEARCH CONSENT FORM Protocol Title: 1565GCC: Multi center phase 1/2 study of combination therapy with the DNA methyltransferase inhibitor decidable and the poly ADP ribose polymerase (PART) inhibitor
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Read and understand the content of the research consent form protocol.
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Who needs research consent form protocol?

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Researchers who are conducting a study that involves human subjects.
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Participants who are involved in the research study and need to give their informed consent.
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Research consent form protocol is a set of guidelines and procedures to inform individuals about the research study, obtain their voluntary agreement to participate, and protect their rights and welfare.
Researchers, institutions, and ethics committees conducting research involving human subjects are required to file research consent form protocol.
Research consent form protocol should be filled out by providing concise and clear information about the study purpose, procedures, risks, benefits, confidentiality, voluntary participation, and contact information.
The purpose of research consent form protocol is to ensure that participants understand the nature of the study, voluntarily agree to participate, and their rights and welfare are protected.
Research consent form protocol must include study purpose, procedures, risks, benefits, confidentiality, voluntary participation, and contact information.
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