Human Factors Engineering Congress to Address Medical Device Design Challenges

Medical device manufacturers and healthcare technology professionals will gather in Philadelphia for the 6th Human Factors Engineering & Usability Studies Congress, organized by Dynamic Global Events (DGE), to examine critical advancements in product design and user experience. The two-day conference, scheduled for May 15-16, 2025, will focus on improving medical device design, combination products, and instructional materials to meet increasingly complex regulatory requirements. Participants will have opportunities to learn from top industry experts about strategies for enhancing user experience and safety in healthcare technologies.

Human factors engineering has become increasingly important in medical device development, as manufacturers seek to minimize user errors and improve overall product interactions. The congress will provide a platform for professionals to share insights, research, and innovative approaches to designing more intuitive and user-friendly medical technologies. By addressing challenges in usability and design, the conference aims to contribute to the ongoing evolution of medical device development. Participants will gain valuable knowledge about regulatory compliance, user-centered design principles, and emerging trends in human factors engineering.

The importance of this gathering stems from the growing recognition that medical device usability directly impacts patient safety and treatment outcomes. As regulatory bodies like the FDA place greater emphasis on human factors validation, manufacturers must demonstrate that their products can be used safely and effectively by intended users in real-world settings. The conference addresses this critical need by providing practical guidance on integrating human factors principles throughout the product development lifecycle.

This matters because medical device errors continue to be a significant concern in healthcare, with usability issues contributing to adverse events and product recalls. The congress represents an important opportunity for industry professionals to collaborate on solutions that can reduce these risks. By focusing on user-centered design approaches, participants can develop medical technologies that are not only compliant with regulations but also genuinely meet the needs of healthcare providers and patients.

The implications of this conference extend beyond immediate design improvements to broader healthcare system impacts. Better designed medical devices can lead to reduced training time for healthcare professionals, decreased error rates, improved patient outcomes, and potentially lower healthcare costs. As medical technology becomes increasingly complex, the human factors engineering principles discussed at this congress will be essential for ensuring these advanced technologies remain accessible and safe for all users.