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Serving Medical Device and IVD Manufacturers in 50+ Countries Worldwide
With experts and labs located throughout the US, Europe, and Japan, NAMSA is ready to support you no matter where you are located.
Contact UsAdvancing Medtech Breakthroughs and Safety Worldwide
Services We Offer
Unmatched Experience in Numerous Therapeutic Areas
Our team conducts testing, preclinical research, and clinical trials on 100,000+ medical devices each year. From stents to SaMD, we’ve seen it all and we know what the US FDA, EU Notified Bodies, and other global regulators expect from you. Patient and user safety has always been a top NAMSA priority and our team of 1,400+ professionals in North America, Europe, and Asia have the expertise to ensure your medical device is safe, effective, and compliant.
About NAMSA
Companies Trust NAMSA to Get It Right the First Time
1967
Year NAMSA Was Founded to Serve Medical Device Companies
270
Medical Device and IVD Clinical Trial Projects Last Year
3,000
Medical Device & IVD Manufacturers Supported Last Year
118,000
Medical Devices Tests Conducted Last Year
100% Focused on Medical Device and IVD Safety and Compliance
Consulting & Strategy
We provide a wide range of strategic consulting services, from regulatory strategy to post-market support. Our team can assist with medical device biological evaluation plans and reports, CERs, FDA 510(k) and PMA submissions, QMS compliance, PMCF surveys, and market research as a single project or as an extension of your team.
Preclinical Research
NAMSA has more experience with more devices than any other company focused on medical device research. That equates to unparalleled preclinical laboratory support for sponsors at our GLP-compliant and AAALAC-accredited facilities in the United States and Europe.
Clinical Research
Our medical device clinical trial consulting expertise spans every manner of technology, therapy, indication, and geography. This broad range of experience allows us to guide our clients through all phases of clinical research. NAMSA’s global footprint also provides clients direct access to local networks to conduct safe, effective, and efficient clinical trials.
Medical Device Testing
Our state-of-the-art labs conduct over 118,000 biocompatibility, microbiology, sterility, and other tests annually. We take pride in managing all medical device testing services in-house to ensure direct oversight of test articles. NAMSA test results are trusted by the US FDA, European Notified Bodies, and other global regulatory authorities.
Shorten Your Time to Market with Support from Concept to Commercialization
Manufacturers lose valuable time hiring different companies to conduct their preclinical research, clinical trials, testing, and regulatory submissions. While each partner may be competent, the unfortunate result is that nobody can offer you a holistic view of your path to compliance, how long it will take, and how much it will cost. NAMSA offers all of these services and can confidently deliver a detailed regulatory roadmap for your device, from preclinical research to postmarket compliance. You’ll avoid wasting time between phases, increase your chance of success, and ultimately save money.
Why Clients Choose NAMSA
I worked with [the NAMSA team] to create a biocomp plan for a complicated combination product. They did an excellent job to help us create a solid plan for testing the device that made sense. They did this in a professional manner and listened to my concerns regarding the previous testing we had done. They all delivered a superb product and we couldn’t be happier.
Bioengineered Human Organ Manufacturer based in the United States1400+ NAMSA Specialists Are Ready to Serve You
Our deep technical and strategic expertise makes us the preferred choice for medical device and IVD manufacturers in the US, Europe, Japan, and beyond. Meet the people who make NAMSA unique.
Meet the NAMSA Team
NAMSA Facilities
Areas We Serve
