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May 20, 2011 ... from and transferred to case report forms (CFS). This module will outline appropriate clinical research practice ... Physical exam findings.
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Documentation in clinical research refers to the written records and reports of the study protocol, procedures, and results.
The Principal Investigator, sponsors, and regulatory authorities are required to file documentation in clinical research.
Documentation in clinical research can be filled out by accurately recording study data, following regulatory guidelines, and ensuring data integrity and confidentiality.
The purpose of documentation in clinical research is to provide a transparent record of the study conduct, data collection, and results for regulatory and scientific review.
Documentation in clinical research must include details of the study protocol, informed consent process, adverse events, and study results.
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