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Audits and Inspections of Clinical Trials of Drugs and Biologics Quiz Complete with Answers Verified and Graded
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When the FDA conducts an inspection, the inspectors will: Review regulatory records. The overall goal of monitoring, audits, and inspection activities is to: Ensure the protection of human research subjects and data integrity. According to ICH E6 GCP, an "Audit" is defined as: A systematic and independent examination of trial-related activities and documents. OHRP is an oversight body primarily concerned with: Protection of human research subjects. According to ICH E6 GCP, an inspection is defined as: An official review of documents, facilities, records, and any other resources related to a clinical trial.
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Audits And Inspections Of Clinical Trials Of Drugs
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Audits and Inspections of Clinical Trials of Drugs
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audits and inspections of clinical trials of drugs
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when the fda conducts an inspection the inspector
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