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 ...

Developing a drug delivery device requires strategic early-stage investments to ensure long-term success and cost efficiency. This whitepaper highlights six critical areas essential for the successful ...

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

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 ...

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.

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 ...