Patrick has 13 years of experience in manufacturing, regulatory/quality assurance and clinical in many industries including: medical device, pharmaceutical, aerospace, telecommunications, food and beverage, and general manufacturing services.
A former Director of QA/Regulatory and Clinical Development, Patrick’s expertise includes compliance assistance, submissions, auditing, clinical design and management, program management, process and product validation, and process improvement (re-engineering) consultation.
Patrick has extensive auditing experience, having been involved in 13 FDA and more than 30 ISO-related audits.
