Modernizing Product Lifecycle Management in Medtech

Medical device companies are under growing pressure to bring increasingly complex products to market faster while maintaining design control, regulatory compliance, and end-to-end traceability. At the same time, aging product lifecycle management (PLM) platforms and vendor-driven technology changes are prompting many organizations to reassess whether their current product development foundation can support today’s requirements. 

Join us for this valuable session to explore how medtech organizations are approaching PLM as more than a standalone engineering system. See how it can be used to connect product data, requirements, quality processes, and manufacturing workflows across the device lifecycle. We’ll examine how leading teams are strengthening collaboration between R&D, quality, regulatory, and operations while using simulation and AI to reduce development cycles and support more informed decisions. 

You’ll learn: 

• Why PLM disruption is prompting a broader reassessment of medtech product development systems and processes 

• How connected product data can strengthen design controls, traceability, risk management, and regulatory readiness 

• How PLM can support the transition from product design and regulatory approval to controlled manufacturing 

• What it takes to establish a reliable source of truth across R&D, quality, regulatory, and operations 

• How simulation and AI can reduce physical iterations, identify potential issues earlier, and accelerate product development