David Teicher, M.Sc., J.D.
Dave has a thirty-five year career specializing in FDA regulatory affairs. His practice focuses on regulatory strategies, preparing domestic submissions, and creating and implementing quality systems for compliance with FDA’s QSR and international regulations and standards.
Dave started his career as an investigator biomedical engineer in the FDA’s Los Angeles and Minneapolis District Offices where he conducted approximately 300 quality assurance audits of medical device manufacturers in the United States and internationally including manufacturers of cardiac pacemakers, mechanical heart valves, angioplasty catheters, dialysis, anesthesia and respiratory care equipment, and intraocular lenses. He then worked for private industry in management roles at various medical device companies. Dave also taught for the graduate level Regulatory Affairs and Services program at St. Cloud State University as an adjunct assistant professor.
Dave earned his Juris Doctor from the Mitchell Hamline School of Law, his Master of Science Biomedical Engineering from the University of Southern California, and his Bachelor of Science in Biology with a minor in Chemistry from San Diego State University.
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