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 ...

The MarketWatch News Department was not involved in the creation of this content. Arlington, Virginia--(Newsfile Corp. - November 18, 2025) - How medical professionals interact with medical devices is ...

Kidd & Co-backed NexPhase Medical Devices has acquired Proven Process Medical Devices. The deal expands the platform’s expertise in R&D, engineering, design and manufacturing of FDA Class II and III ...

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 ...

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 ...

Medical LSR molding simulation prevents defects, reduces costs, and ensures regulatory compliance for device manufacturers.

Newly revised "model contract language" guidance from the Health Sector Coordinating Council provides an updated reference document to help healthcare ...

Association for the Advancement of Medical Instrumentation Brings Human Factors Guidance up to Date Arlington, Virginia--(Newsfile Corp. - November 18, 2025) - How medical professionals interact with ...