Blogs

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 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

November 28, 2025
Building the Foundations of a Modern, Connected Healthcare Ecosystem

Healthcare is undergoing one of the most profound transformations in its history. The challenges are unmistakable—rising costs, aging populations, chronic dis

November 12, 2025
Human-Centred Medical Device Design for Modern Medical Environment

Safety is the most important priority in the medical device industry across the world. Over the last few years or so, a new approach called human-centred design

October 31, 2025
From Sensors to Cloud: The Journey Of IoT Data

The Internet of Things (IoT) has revolutionized the way devices communicate, collect data, and make decisions. The core of this revolution is the ever-expanding

October 10, 2025
IoT Security in US Healthcare: Balancing HIPAA Compliance and Medical Device Innovation

What happens when the hunger for IoT-driven breakthroughs in healthcare runs headfirst into HIPAA’s unbending rules? That’s the urgent and delicate puzzle U

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