Article 16 of the European Union’s Medical Device Regulation and In Vitro Diagnostic Regulation specifically address the ...

In the medical device industry, FDA inspections are not a regulatory hurdle — they are a powerful tool for improving product quality, operational efficiency, and patient safety. Shift from a reactive ...

Experience the next generation of biopharma innovation with PharmaLok™ ZerO sanitary clamps. Designed to simplify and streamline biopharma processes, these advanced clamps feature a universal fit and ...

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

The updated requirements for post-market surveillance (PMS) under the EU Medical Device Regulation (MDR), EU In Vitro Diagnostics Regulation (IVDR), and the U.K.'s forthcoming Statutory Instrument (SI ...

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 ...

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 ...

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 ...