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BIMO Considering Random Sampling Of Clinical Investigator Audits

This article was originally published in The Gray Sheet

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Executive Summary

FDA's Bioresearch Monitoring division is considering the random sampling of clinical investigator inspections in the future, according to staffers at the Center for Devices and Radiological Health.
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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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