For more than 40 years, NAMSA has been the world leader in the safety evaluation of medical devices.
We serve the regulated health care industry, offering testing services and products to device manufacturers, raw material suppliers, pharmaceutical companies, sterilizers and related businesses.
We work with our clients to develop individualized testing programs, guiding them through the simplest test or the most complex development project. We also provide guidance through the submission and regulatory approval process.
The result: a shorter, simpler, and cost-effective path to market.
We understand your world
Delivering a product to market can be a long process, even when you’re familiar with the regulatory requirements. But when you face the unknown requirements of another country, the process can be even more complex. We're a trusted advisor to our clients, offering the best in consulting and testing services, helping them navigate regulatory pathways all over the world.
Reliable results — easily understood
Our technical specialists provide reports and supporting data that are easy to understand and presented in ways that are preferred by regulatory bodies. And we provide services to interpret test results and identify problems that may occur at any point during the product development process.
NAMSA provides consultation throughout the product development life cycle. We develop specific testing programs for your products and provide continued support through regulatory submission, defense and approval.
Committed professionals
We believe our success is the result of a precise, intentional blending of valued teams, world-class testing and advisory services and innovative solutions — a mix that keeps our clients coming back to us again and again.
That's why we create teams of knowledgeable sales professionals, scientific experts, and laboratory staff who, by pooling their expertise and experience, are equipped to deliver smart solutions and on-time results to our clients every time.
