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 ...

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 ...

Unpack the complexities of Section 524B, a key legislative directive aimed at fortifying cybersecurity measures within the ...

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.

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 ...

This week, FDA issued a safety communication connected to Zimmer Biomet’s CPT Hip System Femoral Stem after finding increased risk of thigh bone fracture — postoperative periprosthetic femoral ...

The increasing use of technology in medicine has created cybersecurity vulnerabilities that threaten healthcare systems and patient outcomes. Medical devices are particularly susceptible to attacks ...

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 ...

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 ...

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 ...