Resource clarifies NSF GMP, USP Verified, and FDA cGMP standards and how GMP certification drives trust, retailer ...

很多中国医疗器械厂商在办理 FDA CFG‑NE 证书时都会困惑：CFG‑NE 明明是 “非从美国出口” 的自由销售证书，为什么 FDA 还要求产品必须真实出口美国？ 结合 FDA 官网与 FD&C Act ...

FDA issued a proposed rule today to increase fees for color additive certification services. If finalized, it will implement a 10-cent-per-pound increase in color certification fees and revise the ...

According to the Food and Drug Administration (FDA), the traditional paradigm of medical device regulation was not designed for adaptive artificial intelligence and machine learning technologies. As a ...

The Apple Watch series AFib feature has received new approval from the FDA. From now on, the results returned by the devices are considered medical grade. Previously, the results could be considered ...

Healthcare systems in North America and Europe are increasingly favoring suppliers who can provide “one-stop” solutions—meaning products that transition seamlessly from emergency stabilization to long ...

An Instagram ad catches your eye. You click to the product’s website and find reassurance: The product, it says, is "FDA certified" or was "produced in an FDA registered facility." Mention of the U.S.