From concept to post-market, NAMSA’s Product Development Strategy (PDS) service offering provides proven solutions to assist clients with any development challenge, therapeutic area, reimbursement issue or regulatory environment.
NAMSA is the pioneer of the medical device testing industry and continues to serve as the global marketplace leader for reliable, proven testing services.
The global medical device landscape is complex. Getting a new product or therapy approved requires compelling clinical evidence. At NAMSA, we know what you’re up against and understand how to set you up for success.
NAMSA offers a full range of preclinical research solutions for imaging, data collection, pathology and histopathology.
NAMSA is the industry leader in driving successful regulatory submissions and outcomes through effective, daily interactions with the U.S. FDA, Japan’s PMDA, Europe’s EMA, and China’s NMPA, as well as other international Notified Bodies.
NAMSA offers a full continuum of reimbursement services and solutions for new and existing medical technologies. Our teams are expert in all aspects of reimbursement strategy, including: payer relations, medical policy research, coverage advocacy, HCPCS and CPT code analysis/applications and health economic analysis.
NAMSA’s stand-alone IVD business unit, the only within the Contract Research Organization (CRO) industry, is focused on meeting the unique product development needs of IVD manufacturers.
NAMSA’s Medical Research Organization (MRO®) Program is designed to accelerate great ideas into great medical products that advance healthcare today and into the future.
NAMSA’s medical device experts work across a multitude of therapeutic areas including Cardiovascular, Peripheral/Vascular, Orthopedics, Dental, Neurology, Dermal/Wound Care, General/Plastic Surgery, Ophthalmology, IVD and more.
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