A GCC is not a one-time project, it’s a Long-Term Operating Model
Everywhere we look, companies are announcing new Global Capability Centers. New service providers are springing up. New leaders are offering “plug-and-play”
Everywhere we look, companies are announcing new Global Capability Centers. New service providers are springing up. New leaders are offering “plug-and-play”
DSCO released a draft Guidance Document that establishes how medical device software will be regulated under IMDR 2017. For manufacturers developing medical sol
Imagine a service environment where issues are predicted before they occur, tickets sort themselves, and common problems are fixed automatically, all without hu
AI is transforming MedTech engineering—but only when applied responsibly. In an industry where patient safety, regulatory compliance, and auditability
Medical device design and medical device engineering are twofold interconnected disciplines within the sphere of healthcare technologies. Both with their own di
February 2, 2026. This date marks a regulatory milestone that will reshape how medical device manufacturers approach quality management, documentation, and desi