If you haven’t made the connection yet, you’re in trouble.
When assessing the root cause of a use error, look at the user interface before pointing fingers.
Much of this involves communicating with your customer, and doing it often.
FDA’s perspective on human factors and usability engineering has evolved.
Forty-three percent of pharma and life sciences executives now support FDA evaluating drugs and devices based on both clinical and economic effectiveness.
How can regulatory engineers help integrate regulatory requirements into the design and development process?
Quality should be considered at all stages of production, starting at the earliest stages of product design, says Dr. Vinny Sastri, President of Winovia LLC. Quality System Regulations Series Reports Sponsored by
Which materials make the most sustainable sense and for what applications? How can we create products that balance function with recycling opportunities? With new materials available and on the horizon, the balance point is shifting toward a place that’s more sustainable.