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Smart technology enables data-driven approach to EU MDR/IVDR

The European Union’s Medical Device Regulations (EU MDR) and new regulations for In Vitro Diagnostics (IVDR) represent the most important shift in patient and product safety regulations in over a decade. Grant Thornton’s SmartMDR and SmartIVDR cloud-based project management tools unite functional groups and data for a holistic view into compliance efforts. Watch our video to learn how our solutions can help your organization prepare for and comply with the latest EU regulations.

Sector leaders

Whether navigating through unexpected change, new regulations, or simply trying to better understand the current and future state of the industry, you need a partner with proven experience and a track record of success. That’s where we come in.