Brian D Garthwaite
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Detailed Analysis
Brian D Garthwaite meticulously examines documentation, validation records, training programs, and facility/equipment design to ensure adherence to regulatory standards. He places high importance on addressing and preventing microbial bioburden, conducting thorough complaint investigations, and maintaining comprehensive records to support process validations.
Brian D Garthwaite is a detail-oriented FDA auditor with a keen focus on manufacturing processes, validation, corrective and preventive actions, complaint management, sample testing, training, facility and equipment management, material receipt & handling, cleaning validation, and document management. He prioritizes thorough documentation, validation, and training to ensure compliance with regulatory standards.
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