NAMSA建立于1967年，至今已经有40多年的历史，是全球医疗器械安全性和有效性研究领域中公认的先驱。早在美国FDA 1976年对医疗器械建立比较完整的监管法规之前，就在美国市场中为科学家对医疗器械安全性和有效性研究提供各种实验室测室测试研究服务。
如今NAMSA为医疗器械厂商提供全程产品开发研究、风险管理、和质量管理的实验室数据测试、临床研究计划实施和 法规的咨询服务。服务的领域涉及几乎所有医疗器械产品，例如心血管、骨科、眼科、牙科、诊断试剂等等。
在全球医疗器械安全研究领域，NAMSA始终处于学术的*前沿。很多研究成果被全球标准组织采纳，作为各国医疗器械安全监管的基础。
NAMSA is a medical research organization providing expert regulatory, laboratory, clinical, and compliance services to medical device and healthcare product manufacturers. At every stage of the product development process, we provide strategic guidance and tactical support to help clients commercialize medical products in the major markets of the world.
We serve as your trusted partner, using our insight to identify strategies for saving time, while never compromising quality. We know that compromised quality can quickly take your product right back to the starting line. That’s why it’s so important to have a smart strategy from the outset—and why we put it at the forefront of every project.
The path to regulatory approval can be long and complex. We provide a reliable way to get there.
