Patrick D Stone
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Detailed Analysis
Investigator Patrick D. Stone is methodical and dedicated to regulatory oversight of research protocol compliance, with a keen eye for identifying lapses in record-keeping and deficiencies in IRB approvals.
FDA Investigator Patrick D. Stone pays heightened attention towards the ethical compliance of the clinical trials he monitors. His focus areas includes, but are not limited to, the initiation/continuation of clinical investigations with appropriate Institutional Review Board (IRB) approval, maintenance of research proposal records, and proper documentation of IRB's written procedures.
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