NAMSA started from modest roots as a small medical device testing lab in 1967. Today we serve more than 3,000 companies each year, offering a full spectrum of medical device testing, preclinical/clinical research, and regulatory compliance consulting. Our goal then, as now, is to advance the safety of medical devices for patients and users and to help our clients bring life-saving new medical technologies to market. Our team of 1,400+ scientists, technicians, and consultants are dedicated to delivering clients with strategic guidance and tactical support to fast-track commercialization and make an immediate impact on patient care.
Manufacturers spend years and tens of millions to get a new medical device to market, so working with experienced partners is a must. That’s why more than half of all new FDA Premarket Approvals for innovative high-risk devices are entrusted to NAMSA for testing or clinical research every year. We assist in the following areas:
All Services
Through our offices in the US, Germany, France, Belgium, Spain and Japan, NAMSA supports companies from more than 50 countries around the globe.
See Our Locations
Meet our expansive team of scientists, clinical specialists, and regulatory consultants based in the US, Europe, and Japan.
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