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China Releases Regulations for the Supervision and Administration of Medical Devices (No. 680)

On May 19, 2017, China’s State Council issued the “Supervision and Regulation of Medical Devices (No. 680),” just three years following the State Council Decree No. 650, which addressed similar regulations, including how medical devices should be supervised. While there are many parallels between the two regulations, there are three significant areas of change that … Continued

Risk: An Emerging Driver for New Regulatory Requirements

Risk management is a relatively young management concept. During the last ten to 15 years, it has evolved from a technical economic discipline with roots in insurance, finance and engineering into a central theorem that has permeated regulatory and management domains. Increasingly, it is becoming one of the main topics of conversation, and marketplace catalyst, … Continued

NAMSA Celebrates 50 Years of Scientific Innovation in the Medtech Industry

The world’s only Medical Research Organization (MRO) marks a half century of delivering superior results to global medical device clients and improving patient health. June 6, 2017 – TOLEDO, Ohio – NAMSA, the world’s only Medical Research Organization (MRO®) that accelerates medical device development through integrated laboratory, clinical and consulting services, will celebrate its 50th … Continued