Our Medical Systems evaluations:
- Limit the potential for human error
- Increase effectiveness and ease of use
- Develop User Interface Design and Rapid Prototyping
- Meet government requirements and standards (i.e. FDA and QSR)
- Facilitate delivery of the highest quality care possible
Our medical human factors practitioners are leaders in the industry and are board certified. We have experience working with medical companies that are international as well as start-up companies. PSE provides field evaluations, design interfaces, and human performance studies of medical devices in their use environment. We have an in-house federally approved Institutional Review Board which reduces the time required for study authorization.
Projects
We can effeciently identify the best data collection methods to meet client needs. Our facilities enable us to conduct large focus groups as well as individual studies. Click to see more.
Device Labeling and Documentation
Device labeling and documentation is critical for reducing the potential of human error. Click to see an example.
Instruction Materials and Training
Our medical training and instructional materials have included everything from narrated, multimedia programs for web and CD delivery, to product inserts illustrating step-by-step procedures. Click to see some examples.
Evaluating tasks for their susceptibility to human error and developing methods to reduce error rates is a critical part of our medical human factors experience. Click to see an example.
A key part in enhancing usability and reducing the potential for error is good interface design. Click to see an example.
