GMED and its subsidiaries GMED North America and LNE-GMED UK support manufacturers of medical devices (MDs) and in vitro diagnostic medical devices (IVDMDs) in their certification projects, whatever the level of product risk or innovative technologies used.
As a Notified Body and Certification Body, GMED is internationally recognized for its experience in conformity assessment of medical devices and quality management systems (CE marking, QMS certification, MDSAP program, UKCA marking).
Present in Europe and North America, we serve the medical device and in vitro diagnostic medical device industry worldwide, with strategically located resources (Asia, Israel…).
GMED actively contributes to all governance and standardization bodies, providing its customers with all the technical and regulatory information they need, through the publication of guides, and the organization of training courses, webinars and forums. The GMED Training Center offers its expertise at the service of MD and IVDMD manufacturers, providing them with the technical and regulatory knowledge they need to market their MDs and IVDMDs.
Choose GMED to achieve your MD marketing objectives!