Primary Job Title Vice President of Regulatory Affairs & Quality Assurance Primary Organization 
Advanced Cell Diagnostics
Location San Francisco, California, United States Regions San Francisco Bay Area, West Coast, Western US Gender Male
Website www.acdbio.com/ LinkedIn View on LinkedIn X (Twitter) View on X
Tony brings more than 30 years of experience in regulatory and quality affairs to Advanced Cell Diagnostics.
Over the course of his long career, he has served in many critical management positions, including VP and Director roles for regulatory and quality assurance with leading pharmaceuticals, biologics, and diagnostics companies like Thermo
Fisher, Siemens, Johnson & Johnson and Novartis.
Most recently, he served as VP of Regulatory and Clinical Affairs for Qiagen in Molecular Diagnostics. Within in vitro diagnostics, Tony specialized in immunodiagnostics, clinical chemistry, IHC, molecular diagnostics, pharmacogenomics and companion diagnostics.
In addition to these managerial roles, Tony has also overseen many successful FDA premarket approvals, from DAKO's HercepTest companion diagnostic to Genentech's Herceptin, as well as molecular diagnostics for pharmacogenomics from companies such as Celera Diagnostics and GE Healthcare.
He was also instrumental in working with Precision Therapeutics, LabCorp and Quest CLIA labs. As an expert in quality management, Tony accomplished efficient turnaround compliance with quality systems of US QSR and ISO 13485 for Hologic, Agilent Tech, Novartis, Quest, Thermo Fisher, and Life Technologies.
Tony received a BS in Microbiology/Molecular Biology and a MS in Immunology and Genetics from the University of Oklahoma.
