Blogs

January 06, 2026
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”

December 22, 2025
CDSCO Medical Device Software: Regulatory Pathways and Classification

DSCO released a draft Guidance Document that establishes how medical device software will be regulated under IMDR 2017. For manufacturers developing medical sol

December 16, 2025
From ITSM to CSM: How a Telco MSP Cut Complaints by 40% using ServiceNow and Agentic AI

Imagine a service environment where issues are predicted before they occur, tickets sort themselves, and common problems are fixed automatically, all without hu

December 12, 2025
What AI Can — and Cannot — Do in Regulated MedTech

AI is transforming MedTech engineering—but only when applied responsibly. In an industry where patient safety, regulatory compliance, and auditability

December 10, 2025
Medical Device Design and Medical Device Engineering

Medical device design and medical device engineering are twofold interconnected disciplines within the sphere of healthcare technologies. Both with their own di

December 09, 2025
Quality Management System Regulation (QMSR) - What’s Changing in Medical Device Regulation

February 2, 2026. This date marks a regulatory milestone that will reshape how medical device manufacturers approach quality management, documentation, and desi

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