conformity assessment

Rising product recalls and growing regulatory complexity are putting new pressure on engineering education. This article makes the case for integrating product safety compliance into university curricula — and outlines what a comprehensive program should include.

After years of regulatory complexity, the EU Commission offers medical device manufacturers a path forward: proposed changes limit AI Act requirements for devices, streamline risk classifications, and create efficiencies that could reduce costs and speed innovation.

When the FCC issued FCC 16-74 and extended the 2.948 Listing program, the pressure driving US-China MRA negotiations evaporated with it. Unpack what the ruling actually says, what the KDB fine print reveals, and whether any real leverage remains for moving MRA talks forward.