EU-MDR presents a compelling opportunity for medical devices makers to shift from managing documents to a product centric approach to their PLM investments. 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 along with existing and emerging regulations.
Join this webcast to hear Inspirage, a Medical Device / Life Science industry expert share best practices for:
Architecting PLM for future regulatory compliance
Solution Architect Lead, PLM and MDM,
PLM Life Sciences Leader,