A medical device manufacturer sought HF engineering support to develop HFE deliverables and conduct a validation study for an aesthetics device.
Improve usability and safety of wearable pump for Type 2 Diabetes patients
A medical device manufacturer sought to evaluate the usability and safety of the patch pump and training with potential patients and healthcare providers.
Human factors training course designed for medical device team
A global medical device manufacturer wanted to promote internal awareness of and appreciation for best practices in the application of human factors engineering to medical device development.
Human factors training course designed for FDA
The FDA reached out to the Human Factors and Ergonomics Society (HFES) to assemble a team of experts to provide a training course for the Division of Medication Error Prevention and Analysis (DMEPA)...
Evaluate risk of redesigned surgical equipment
A medical manufacturer had US-approved surgical equipment, but the current design was not working for some international markets.
Iteratively design medical device IFU
A pharmaceutical company needed to evaluate the effectiveness of their instructions for use for a new product.
Prepare HFE documentation for aesthetics device system
A medical device manufacturer sought HF engineering support to develop HFE deliverables and conduct a validation study for an aesthetics device.
Improve usability and safety of wearable pump for Type 2 Diabetes patients
A medical device manufacturer sought to evaluate the usability and safety of the patch pump and training with potential patients and healthcare providers.
Human factors training course designed for medical device team
A global medical device manufacturer wanted to promote internal awareness of and appreciation for best practices in the application of human factors engineering to medical device development.
Human factors training course designed for FDA
The FDA reached out to the Human Factors and Ergonomics Society (HFES) to assemble a team of experts to provide a training course for the Division of Medication Error Prevention and Analysis (DMEPA) from the Center for Drug Evaluation and Research (CDER).
Evaluate risk of redesigned surgical equipment
A medical manufacturer had US-approved surgical equipment, but the current design was not working for some international markets.
Iteratively design medical device IFU
A pharmaceutical company needed to evaluate the effectiveness of their instructions for use for a new product.