August 28, 2019 | 2pm ET
EU-MDR presents a compelling opportunity for medical devices makers to leverage their PLM investments for an advantage. 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.
Join this 60-minute webcast to hear Medical Device / Life Science industry expert, Inspirage, share best practices for: