In the medical device industry, FDA inspections are not a regulatory hurdle — they are a powerful tool for improving product ...

The DEA has announced new rules for remote prescription of controlled substances. As telehealth adoption grows, regulatory ...

One area that medical device manufacturers often overlook in post-market surveillance (PMS) planning for EU MDR and EU IVDR compliance is the role of the supply chain.

From the first stages of development through post-commercialization, medical devices — across all classifications — must clear a complex series of hurdles throughout their total product life cycle.

As the industry continues to see significant growth for drug products developed in cartridges, there is a trend for pharmaceutical companies to evaluate more complex drug molecules, such as biologics, ...

AI-enabled medical devices have become a transformative force in healthcare, offering sophisticated data-driven insights that can enhance diagnostic accuracy, personalize treatment, and optimize ...

As industries demand smaller, more complex components, micro molding has become a crucial technology. Selecting the right manufacturing partner is not just a production decision but a long-term ...

Loveland, CO - Nordson MEDICAL, a Nordson Company (Nasdaq: NDSN), is thrilled to unveil PharmaLok™ ZerO sanitary clamps, an innovative solution designed to replace traditional TC clamps in the ...

A virtual start-up identified a significant opportunity to develop a catheter-based embolic protection device for high-risk patients undergoing transcatheter aortic valve replacement (TAVR). Lacking ...

A leading medical device company recently teamed up with Nordson MEDICAL to redesign a crucial component for a specialized medical device. Initially, Nordson MEDICAL was tasked only with manufacturing ...