Discover how integrated microfluidic pumping solutions eliminate bulky external equipment, simplifying cartridge design while ...

Discover how thinXXS helped Pattern Bioscience accelerate digital droplet chip development through precision manufacturing, ...

Medical device document approvals seem to be a roadblock when you are the most pressed for time. But if the right approvers ...

Imagine a fire sweeping through a forest. It moves quickly, burns through almost everything in its path, produces immense destruction, and changes entire landscapes. It also clears out dead debris and ...

The most expensive decision a U.S. medical device company makes in Latin America is rarely the one its leadership team has on the agenda. It is not the choice of country. It is not the product ...

In micro molding, automation is far more than robotics on the factory floor—it is the manufacturing architecture that enables quality, scalability, and repeatability. While conventional molding ...

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, ...

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.

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 ...