Leaders from Ernst & Young deliver intel on the four biggest trends that impacted the medtech industry in 2024 that savvy ...
The EU AI Act is a landmark legislation that will shape the future of AI in Europe and is expected to be the baseline for ...
Bovine collagen has long been valued as a biomaterial in medical devices due to its biocompatibility, scaffold properties for cell growth, and hemostatic qualities. Despite widespread global use, ...
Consulting and engineering services are available to help meet regulatory requirements for building materials in both Canada and the United States (ICBO & CABO) as applicable... ETL SEMKO, a division ...
The deadline for medical devices compliance to the new medical devices regulation 2017/745 (EU MDR) was originally May 2020 for class l non-sterile devices and May 2024 for all other devices. During ...
Smart implants revolutionize healthcare with embedded sensors for real-time monitoring. Polycarbonate urethanes offer ...
Occlusion testing using robotic automation for medical devices, such as infusion pumps, catheters, IV lines, insulin pumps, ventilators, and other drug delivery systems, involves robotic systems to ...
With the rise AI-enabled medical devices, the FDA is soliciting comments and feedback regarding the importance of AI safety and effectiveness considerations in advance of its upcoming Digital Health ...
All startups must navigate the “Valley of Death” as they transition from initial discovery and ideation to market launch. This critical period, characterized by heightened risk of failure, is ...
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