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CRC POLICY & PROCEDURE Category: Research Responsible Office: Preclinical Research Center Responsible Executive: Director Create Established: 10/26/12 Date Last Revised: Date Posted to Library:INFORMED
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CTRC policy and procedure refers to the rules and guidelines set by an organization to ensure compliance with regulatory requirements and best practices related to the use of human subjects in research studies.
Researchers, institutions, and organizations conducting research studies involving human subjects are required to file CTRC policy and procedure.
CTRC policy and procedure can be filled out by following the specific guidelines and instructions provided by the Institutional Review Board (IRB) or research ethics committee overseeing the study.
The purpose of CTRC policy and procedure is to protect the rights and welfare of human subjects participating in research studies, ensure compliance with ethical standards, and maintain the integrity of the research data.
CTRC policy and procedure must include detailed information about the study protocol, risks and benefits to participants, informed consent process, data management and confidentiality procedures, and any potential conflicts of interest.
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