Medical devices are engineered to solve complex clinical problems. Yet many enter the field without a full accounting for what happens after deployment. Hospitals depend on equipment that performs consistently.

Increasingly, inspectors for the U.S. Food and Drug Administration (FDA) will evaluate your CMMS provider’s security controls—not just your internal procedures.

In today’s energy sector, regulatory complexity isn’t a temporary headache—it’s the new normal.

The digitalization of society during the last decade has created many opportunities for businesses and organizations.

The manufacturing industry is undergoing a transformation driven by rapid technological advancements, changing consumer preferences, and evolving regulatory frameworks.

Early-stage medtech companies are under tremendous pressure to develop quickly, prove value, and obtain regulatory approval or clearance as fast as possible.

All manufacturing companies must manage an ever-growing mountain of priceless inspection data. Yet measurement results, process iterations, and approval reports are scattered across hard drives and USB sticks.

When I first became involved in lean (continuous improvement), I was the VP of operations at a privately held company in the Midwest.

In this article I want to spend time with Søren Kierkegaard. I’ve been interested in his ideas because he occupies an unusual place in the history of thought. He’s considered a pioneer of existentialism, and yet he was also a man of faith.

(TRIMEDX: Indianapolis) -- TRIMEDX has launched TRIMEDX-AIQ, an AI intelligence offering that sets a new standard for clinical asset optimization.