is a Medical Research Organization (MRO), accelerating product development
through integrated laboratory, clinical and consulting services. Driven by our
testing and regulatory expertise, NAMSA's MRO® Approach plays an important role
in translational research, applying a unique combination of
disciplines-consulting, preclinical, toxicology, microbiology, chemistry,
clinical and quality-to move client's products through the development process,
and continue to provide support through commercialization to post-market
requirements, anywhere in the world. Additional information can be viewed at
working in coordination with our in-house Experts, we look for ways to save you
more time and reduce the overall amount of testing. Our technical specialists
partner with you to develop a cost effective program, applying almost 50 years'
experience in medical device safety and regulatory compliance for your benefit. NAMSA was the first
independent company in the world to focus solely on testing medical device
materials for safety. Our mission remains today, as it has been for almost 50
years, to make a scientific contribution to every medical device in the world.
Does your medical device development partner
have a proven track record of success? Read NAMSA's latest case study to learn how our
expert teams assisted biosurgical firm, Biom'Up, achieve PMA status in 2.5
years, saving $17M+ in costs and 23 months in time.