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 to hear Inspirage, a Medical Device / Life Science industry expert share best practices for:

• Configuring Digital Thread PLM processes and data
• Rapidly implementing PLM capabilities using pre-built data models
• Advancing from document management to digital model management
• Creating true single sources of truth for product information across their lifecycles
• Defining a PLM strategy that supports data / fact-based portfolio rationalization and management
• Architecting PLM for future regulatory compliance