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PPM IRB Initial Review Form (revised March 2016) Page 1 of 18 INSTITUTIONAL REVIEW BOARD Initial Review Form Use for Approval of Research Involving Human Participants
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The IRB application for initial is a form used to request approval for conducting research involving human subjects for the first time.
Any researcher or organization planning to conduct research involving human subjects for the first time is required to file an IRB application for initial.
The IRB application for initial must be completed with details about the research study, the potential risks to participants, the informed consent process, and other relevant information.
The purpose of the IRB application for initial is to ensure that research involving human subjects is conducted ethically and in compliance with regulations to protect the rights and welfare of participants.
The IRB application for initial must include information about the research study design, recruitment methods, risks and benefits to participants, informed consent process, and plans for data management and participant confidentiality.
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