Live and on-demand webinars are presented by industry experts and solution providers in the medical industry.
Medical device chemical characterization testing per ISO 10993-18 is often the leading source of delay, cost overrun, and regulatory questions in a manufacturer’s biocompatibility program. Problematic study outcomes tend to be associated with a few recurring issues, with most difficulties arising not from the analytical chemistry itself, but rather from key decisions made throughout the process.
Biotech Startup Turns to Space to Manufacture Artificial Retinas
AI-Designed Shape-Shifting Microneedles Aid Diabetic Wound Healing
Why the U.S. and China Are Taking Different Paths on Pig-to-Human Organs
Where Test Plans Break: Measuring the Performance of Ultra-Miniature...
Why the Next Medical Breakthrough May Come from Space
How Smart Implants and AI Robotics Could Transform Neurological Surgery
Understanding power system components and how to connect them correctly is critical to meeting regulatory requirements and designing successful electrical products for worldwide markets. Interpower’s Ralph Bright defines these requirements and explains how to know which cord to select for your application.
Design for Miniaturization: Meeting the Demand for Smaller, Smarter, and More...
2026 Medical & Healthcare Robotics Summit (Online)
Making Telemedicine Work in Low-Connectivity Environments
Why the Next Medical Breakthrough May Come from Space
How to Avoid Chemical Characterization Pitfalls in Medical Devices
Eurofins Medical Device Testing (MDT) provides a full scope of testing services. In this interview, Eurofins’ experts, Sunny Modi, PhD, Director of Package Testing; and Elizabeth Sydnor, Director of Microbiology; answer common questions on medical device packaging and sterilization.
