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 ...

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 ...

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 ...

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 ...

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 ...

Graphic featuring an image of Masimo CEO Joe Kiani at a podium with the company logo in the background and headshots of newly elected board members. The medical device sector must meet stringent ...