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 ...
Enter your credentials below to log in. Not yet a member of Med Device Online? Subscribe today.
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 ...
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 ...
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 ...
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 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback