Accompanying you in the transition to the European Medical Device Regulation
GMED, and its subsidiaries GMED North America and LNE-GMED UK, provide comprehensive solutions to support you throughout the certification of your medical devices (MDs) and in vitro diagnostic medical devices (IVDs).
GMED, and its subsidiaries GMED North America and LNE-GMED UK, provide comprehensive solutions to support you throughout the certification of your medical devices (MDs) and in vitro diagnostic medical devices (IVDs). These assets ensure the success of your projects, regardless of the product's risk level or the innovative technologies used.
GMED, as a Notified Body, provides expertise in assessing the conformity of your devices to European regulations for their marketing in the EU. New certification slots are also now available.
Our support in the transition ensures a comprehensive range of services. We evaluate the compliance of your MDs and IVDDs (CE marking, UKCA marking) and quality management systems (QMS certification, AI QMS certification, MDSAP, TCPIII...).
You can contact our sales team now to discuss your testing and certification projects.
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