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National Marrow Donor Program Institutional Review Board
IRB Registration: IRB00001253Assurance: FWA00000441Notice of Action
Date: July 12, 2018Study Number: IRB19910002Meeting Date: July 12, 2018,
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What is 6 protocols and consent?
6 protocols and consent refer to the procedures and agreement required for conducting research involving human subjects.
Who is required to file 6 protocols and consent?
Researchers and institutions conducting studies involving human subjects are required to file 6 protocols and consent.
How to fill out 6 protocols and consent?
To fill out 6 protocols and consent, researchers need to provide detailed information about the study design, potential risks and benefits to participants, and obtain informed consent from participants.
What is the purpose of 6 protocols and consent?
The purpose of 6 protocols and consent is to ensure the ethical treatment of human subjects in research studies, protect their rights and welfare, and obtain their voluntary participation.
What information must be reported on 6 protocols and consent?
Information such as study objectives, methodology, potential risks, benefits, confidentiality measures, and informed consent process must be reported on 6 protocols and consent.
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