Posts

Video Capture and Analysis: 5 Ways You’re Hurting Your Video Analysis

This blog post is part two of a two-part series on using video records in contextual inquiry.

In part one Video Capture and Analysis: 5 Reasons to Film Your Research,” we discussed five reasons to film your research. One of the biggest advantages of filming your research is that you can analyze the video after the research has concluded.

In video analysis, you codify behaviors or events to put quantitative values to qualitative observations. These quantitative values can be a useful way to quickly and simply communicate your findings. Video analysis has been a staple of behavioral research methods for a long time, but there’s surprisingly little information about how to do it effectively. Read more

Video Capture and Analysis: 5 Reasons to Film Your Research

This blog post is part one of a two-part series on using video records in contextual inquiry.

Design Science researchers almost never go into the field alone—we’re accompanied by a videographer, who may be carrying up to 5 cameras. The ability to film in restricted areas like operating rooms and catheter labs is something that sets Design Science apart, and with good reason: it’s difficult to gain permission to film in an operating room. It requires long-standing relationships with surgeons, physicians, nurses, and the medical facilities they work for. These relationships are built on complicated, time-consuming navigation of hospital approvals, and repeated positive experiences with our researchers and videographers. Read more

Image: Flowchart

MDO Article: “How To Know You’ve Passed Validation Testing (And What To Do If You Haven’t)”

Understanding the ramifications of less-than-perfect validation testing results can be complex. In his recent article for Med Device Online, Peter Sneeringer presents 6 questions to help companies decide if errors seen during testing indicate a likelihood that the FDA will reject their submission.
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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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Design Internship Opportunity

Are you a designer with a passion for user research? Design Science is seeking an intern with a background in industrial or graphic design to work in our information design department.

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Steve Wilcox Co-Writes AAMI Guidance

A new guidance for medical-device field research has just been released: the Technical Information Report, AAMI TIR51:2014, “Human factors engineering – Guidance for contextual inquiry.”

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Great Minds Think…Differently?

Recently at DS, we thought it would be fun for the whole office to take the Myers-Briggs personality assessment (despite one office manager’s insistence that she was far more complex than four letters!).

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It’s Here! Design Science Launches New Website

We’re thrilled to announce the launch of our new and improved website! Dscience.com is now cleaner, faster, and—most importantly—responsive.

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