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THE NONEVENT FOCUSED ON GCP INSPECTION READINESS IN THE EU!EUROPEANCLINICAL TRIALSINSPECTION READINESSSUMMITImprove Inspection Readiness Through Maximizing Document Quality and Accessibility and Enhancing
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Inspection readiness - exl is the state of being prepared for a regulatory inspection by the FDA or other governing body.
All pharmaceutical companies and manufacturers are required to file inspection readiness - exl.
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Information such as facility policies, standard operating procedures, training records, and batch records must be reported on inspection readiness - exl.
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