On-demand webinars presented by industry experts and solution providers in manufacturing, medical, aerospace, military, and commercial industries.
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
In collaboration with the Fort Wayne Metals Engineering team, Eric Dietsch focuses on supporting customers with material recommendations, product development, and education. Eric is available to help you and your company with any Nitinol-related questions or needs that you may have.
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.
