We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
The FDA’s unique device identification (UDI) rule might improve device tracking but is plagued with unresolved issues such as how to label devices with multiple components. Read More
Sweeping new medical device regulations in the European Union are expected to be finalized in December or early 2017, although medical device manufacturers will still have three to five years to comply. Read More