Kent Conforti
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Detailed Analysis
Investigator Conforti leans towards a meticulous assessment of manufacturing processes with a primary focus on quality compliance and validity of document procedures. He prioritizes the adherence to quality assurance protocols, effectiveness of bioburden control and cleanliness protocols.
FDA Investigator Kent Conforti places strong emphasis on process controls and document integrity. He is especially attentive towards thoroughness and follow-up of discrepancies, compliance with quality assurance practices, and effectiveness of cleaning validation. His auditing style leans towards ensuring regulatory compliance in drug manufacturing processes and primarily concerning bioburden control, equipment maintenance, and quality of records.
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