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 IMDRF’s Standards Working Group issued final guidance on optimizing standards for regulatory use, noting that optimized standards offer a way to streamline regulatory processes as medical devices grow in complexity and international markets expand.
Devicemakers marketing mobile health solutions or other software that help patients manage chronic conditions may see big benefits in coming years, new research suggests.
The China Food and Drug Administration Wednesday announced registration fees for locally made and imported medical devices aimed at speeding up the processing of applications.