Posts

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DS Attends HIMSS 2017

The HIMSS 2017 conference is “the year’s largest and most important healthcare IT conference in the United States” and brings together executives, clinicians, IT professionals, and more for a week of networking, knowledge-sharing, and forward-thinking. Read more

Human Factors and Ergonomics in Healthcare: Shaping the Future

HFES Presentation: Improving IFUs with Eye Tracking, Human Factors, and Design

Are you attending the 2016 International Symposium on Human Factors and Ergonomics in Health Care: Shaping the Future? If so, be sure to check out our presentation on how to improve your Instructions for Use (IFUs). Peter Sneeringer, Director of Human Factors, and Lindsay Carrabine, Design Director, will provide their first-hand perspectives on how to optimize the IFU creation process. Read more

Usability Ecosystem 2.0 graphic

2015 IDSA Medical Design Conference

Join us at the 2015 IDSA Medical Design Conference—the premier medical design event—on October 21 at the Center for Advanced Medical Learning and Simulation (CAMLS) in Tampa, FL.

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Design Considerations for Interconnected Medical Devices

Over the past several years, there has been a drastic increase in the deployment of “interconnected” medical devices (e.g., wireless glucose monitors, infusion pumps, pacemakers, etc.). As our medical devices become more interconnected, they become increasingly critical to clinical decision-making and patient care. Access to information increases, decision making evolves, and, hopefully, patient care improves. Read more

Picture: Grid of different images showing usability testing

MDO Article: “Achieving Realism In Human Factors Work: How To Stay Out Of Fantasy Land”

Designing usability studies that are “representative” is not only necessary for valid data, it’s also an FDA requirement. Chad Uy shares some methods for maintaining realism to ensure representative usability studies in his recent article for Med Device Online.

FDA to Accept Applications for Expedited Medical Device Approval

On April 15th, the Food and Drug Administration will begin accepting applicants through its new Expedited Access Premarket Approval Application for Unmet Medical Needs for Life Threatening or Irreversibly Debilitating Diseases or Conditions (“Expedited Access PMA” or “EAP”). Read more

MDO Article: “4 Proposals To Accelerate The Growth of mHealth”

What 4 things should app developers, traditional medical device and pharmaceutical companies, and regulators do to accelerate the growth of mHealth? Read more

Now Hiring: Research Associates

Are you passionate about working collaboratively to make a felt difference in the world? At Design Science we have one mission – fitting products to people.

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