Lab IoT adoption is growing, and recent innovations make it more promising than ever. See how IoT advances can unlock new ...

The FDA conducts approximately 12,000 domestic inspections and 3,000 foreign inspections each year in more than 90 countries.

Clear and specific IVD intended use criteria are required and introduce significant challenges for manufacturers seeking CE Marking and global market access. With IVDR compliance deadlines approaching ...

The integration of technology and connectivity into healthcare is not only improving patient outcomes but also reshaping the way care is delivered.

Across our industry, IoMT will enable us to conduct research in ways that would never previously have been possible. The Internet of Things (IoT) is revolutionizing the way we live and work. From ...

As technology component pricing continues to rise, MedTech manufacturers are applying proven methods and exploring new approaches to maintain profitability and extend product lifecycles. During the ...

It’s time to consider CAPAs as opportunities rather than just other issues to tackle. For many people working in medical devices, or a similarly regulation-laden industry, CAPA (Corrective Actions and ...

“This cutting-edge technology empowers us with the ability to navigate complex vascular procedures with greater precision, ensuring optimal outcomes for our patients. We are honored to be a part of ...