483
Timothy Pluard, M.D.Timothy Pluard, M.D. – FDA 483, Jun 6, 2006
Record Details
An FDA inspection of Timothy J. Pluard, MD, a clinical investigator in Kansas City, MO, revealed significant deviations from good clinical practices. Observations included a failure to conduct an investigation according to the investigational plan, specifically regarding subject dosing, and a failure to maintain adequate case histories. These issues indicate a lack of control over study conduct and data integrity.
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