Dave Teicher, M.Sc., J.D., Consultant

Dave is a regulatory expert. He has a thirty-five year career specializing in FDA regulatory affairs. He focuses on regulatory strategies, preparing domestic submissions, and creating and implementing quality management 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 including SciMed (Boston Scientific) and Endocardial Solutions. Dave taught for the graduate level Regulatory Affairs and Services program at St. Cloud State University as an adjunct assistant professor.

Dave earned his Bachelor of Science in Biology with a minor in Chemistry from San Diego State University, his Master of Science Biomedical Engineering from the University of Southern California, and his Juris Doctor from Mitchell Hamline School of Law.

In his free time, Dave enjoys attending car shows, racing cars competitively, and spending time at is cabin.