Why International Standards Don’t Explicitly Specify “How”
Why the FDA Standardized the Term “Human Factors Engineering”: Understanding Terminology, Regulatory Expectations, and Current Trends
Why Presubmission is Important
Why Class I Medical Devices Are Subject to Usability Engineering
Understanding the Difference Between Risks and Issues
What is Safety? Why Zero Risk Does Not Exist
Understanding the Three-Step Method
Why Focus on the Probability of Harm Rather Than the Probability of Defects?