Mass consolidation is sweeping up small medtech organizations. Med device startups and early-stage companies that want to be ...

In micro molding, automation isn’t an add-on. Learn how integrated handling, inspection, and packaging enable scalable, ...

In micro medical manufacturing, a prototype that fits perfectly in the lab can still fail at production scale. When device performance depends on leak-tight seals, precise dosing, fluid flow, or ...

FDA has now completed just over 100 inspections under its new Quality Management System Regulation, and the agency has begun sharing preliminary observations from those inspections. Early FDA findings ...

Across industries, innovation platforms constantly monitor device usage and anticipate future needs, fueling breakthrough ideas in real time. AI agents are dissolving silos in large organizations, ...

New operators don’t fail because they’re careless. They fail because the instructions they’re given were never designed for real work on a modern shop floor. Paper binders go out of date. Text-heavy ...

Women’s History Month is a time to celebrate progress, but for those of us in medical technology, it must also be a time of reckoning. While women represent 50% of the global population, a silent, ...

Raising funds in the medical device industry is always challenging. Doing so as a startup can be even more so. And U.S. medical device companies seeking funding this year will find that innovative ...

As liquid biopsies, wearables, multi-omics, and AI mature, diagnostics could become the operating system of healthcare: a continuously learning layer that turns everyday data into earlier action.

Artificial intelligence is rapidly transforming datacenter power architecture. In 2024, racks consuming 60 to 80 kW were already challenging traditional infrastructure assumptions. Today, AI racks ...

As syringe-based products evolve toward higher viscosities and larger fill volumes, longstanding assumptions about dye ingress testing face growing mechanical constraints. Earlier analysis showed that ...

In 2023, the FDA made the electronic Submission Template And Resource (eSTAR) mandatory for most 510(k) submissions. Although eSTAR is not an AI tool, the move was the first definitive leap toward the ...