Medical device design and development is a process that helps to ensure devices that go to market are safe, effective, marketable, and profitable. The process is a blueprint of the phases needed to ...

The Food and Drug Administration (FDA) development and approval process for drugs and medical devices involves multiple phases that ensure the safety and effectiveness of products before and after ...

Product design risks can be mitigated through digital commissioning strategies for device design that speed continuous design ...

At MD&M West 2026, Carl Douglass cuts through the hype to show how additive manufacturing truly accelerates Class II and III ...

Global healthcare systems require medical devices that are safe and effective in diagnosing, treating, and preventing diseases, and physicians rely on a wide range of medical devices to help identify ...

The medical device industry remains a significant force in the global economy, with revenues exceeding $300 billion and a projected annual growth rate of 6%. The United States leads the market, ...

Resonetics experts explain the different stages of nitinol’s journey as it becomes part of a life-changing medical device.

Medical device design and development has evolved over the years, notably influenced by market demands and regulatory requirements. Traditional design practices, beginning with a reliance on generic ...

The Master of Engineering (M.Eng.) in Medical Device Development is a cutting-edge program that promises to accelerate the career development of aspiring engineers in all disciplines who wish to pivot ...

As medical devices become increasingly more complex, the need to enhance development efficiency, quality by design, integrated risk management, and regulatory compliance has never been greater The ...