Medical Device Qualified Supplier Directory
Anatomy of a Good Use Error Risk Assessment
As Human-Centered Design (HCD) continues to drive development of smaller, smarter next-generation drug delivery devices, it is becoming increasingly important for biologics manufacturers to apply human factors engineering (HFE) principles to their selected delivery method or platform. Done successfully, this strategy can lead to safer, more desirable devices that improve patient adherence, save time and money in the manufacturing process, and in many cases give the product a competitive boost. The Use Error Risk Assessment (UERA) is a critical component of the HFE process.
For more information contact Phillips-Medisize, a Molex company
E: [email protected]
T: (715) 381-3344
1201 Hanley Rd., Hudson, WI, 54016, United States