EU-MDR presents a compelling opportunity for medical devices makers to leverage their PLM investments for an advantage. Today’s advanced PLM solutions are architected to manage the digital processes and data related to New Product Development.
The key is to harness PLM advancements in connectivity, data and workflow management technologies. That’s exactly what’s required for timely, error-free and cost-efficient compliance with EU-MDR and other regulations.
Watch this webcast replay to hear Inspirage, a Medical Device / Life Science industry expert share best practices for:
Solution Architect Lead, PLM and MDM,
PLM Life Sciences Leader,