IDC Spotlight: Connected Life-Cycle Management Streamlines Software Development for Medical Devices

As software increasingly becomes a competitive advantage in medical devices, MedTech companies must find ways to accelerate development while staying compliant. This IDC Spotlight Paper explores how Connected Lifecycle Management (CLM) is transforming software development for regulated industries. Learn how CLM streamlines compliance, enhances traceability, and enables modern DevOps practices—empowering R&D and QA/RA leaders to deliver safer, high-quality products faster.

What You'll Learn:

1. How CLM helps life science teams accelerate change management while maintaining compliance with IEC 62304, ISO 13485, and ISO 14971.
2. Why traditional PLM and ALM systems fall short for modern AI/ML-enabled devices—and how CLM bridges the gap.
3. How CLM integrates regulatory compliance into agile workflows while keeping teams in their preferred development tools.

Download the full report to explore how CLM supports AI-driven medical innovation while reducing compliance overhead.