MD+DI Senior Editor Amanda Pedersen calls on investors, industry leaders, and policymakers to prevent the collapse of the medtech ecosystem as we know it.

Understanding the full range of technological options in intervention catheter composite design is essential to meet the ...

Utilizing design for manufacturing (DFM) and tools such as Moldflow® simulation software is also common, but like any process ...

For nearly 10 years, Technical Committee 194 of the International Organization for Standardization (ISO) and its various working groups have been developing the documents known collectively as ISO ...

Duane Morris Silicon Valley office partner Agatha H. Liu, PhD, practices intellectual property law, focusing on IP analysis, portfolio management, and strategic counseling. Drawing on more than 20 ...

The French maker of ophthalmic devices is the largest maker of lenses in the world. It spends 200 million euros (equivalent to $226 million) on innovation annually, and Essilor is also a robust ...

Examining the evolving dynamics between EU and FDA regulations for medical devices. The webinar will address the historical practice of obtaining a CE Mark in Europe first, contrasting it with the ...

Product liability lawsuits can be a big burden on medical device companies. Occasionally, they can be disastrous financially. For instance, Dow Corning filed for bankruptcy in 1995 based on hundreds ...

In an example of innovation across country borders, Paris-based Gecko Biomedical is developing tissue adhesive technology for wound closure and sealing in collaboration with cofounder Dr. Robert ...

As medical technology becomes more sophisticated and interconnected, device security threats escalate to pose risks in patient health and privacy. The U.S. FDA has strengthened its cybersecurity ...

Learn the latest technology for inspecting medical devices at every stage of the development process, from initial R&D through high-volume production with automated end to end workflows.