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 ...

In the medical device industry, usability plays a critical role in ensuring the safety and effectiveness of highly complex medical products. The IEC 62366-1:2015 standard, which focuses on the ...

Averna's Matt Thompson shares strategies to avoid common traps when transitioning medical devices from R&D to manufacturing.

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 ...

Overview Designing and manufacturing precision steerable catheters for complex anatomies requires smart catheter design. Precision engineering plays a key ...

These definitions as written out by AAMI (The Association for the Advancement of Medical Instrumentation) offer clarity, helping designers recognize and address these risks effectively in product ...

The pandemic has forced remote product development in many fields, and the medical device arena has seen rapid growth in the use of virtual reality (VR). Studying the potential outcomes for individual ...

One way to accelerate innovation in recent times has been to use 3D printing. This process lets designers work through more iterations faster to find improvements, while accelerating failure to ...

Dublin, Oct. 13, 2025 (GLOBE NEWSWIRE) -- The "An Introduction to the Design and Development of Medical Devices Training Course (Dec 3rd - Dec 4th, 2025)" training has been added to ResearchAndMarkets ...

Medical device manufacturers are using titanium etching to take advantage of this medtech metal’s many benefits for innovative technologies.

The U.S. Food and Drug Administration (FDA) categorizes medical devices into three classes based on the level of risk the devices pose to patients and users. Image Credit: IGORdeyka/Shutterstock.com ...