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 ...

Successful new medical devices hinge on the designer’s understanding of the specific requirements of the procedures they support, including factors like usage frequency and duration. This is ...

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 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 ...

Design team leader at Owen Mumford, Myles Whiting lifts the curtain and provides an exclusive backstage view of how the R&D department within a successful medical device manufacturer works. Have you ...

D Printing for Medical Devices Training Course (June 17, 2026)" training has been added to ResearchAndMarkets.com's offering. The global market for medical devices and equipment is estimated to have ...

Medical device manufacturing is a high-stakes game where efficiency meets precision. With tight regulations, complex designs, and a need for speed, how do companies stay ahead without cutting corners?

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 ...

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 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 ...

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 ...