Many involved with medical device manufacturing have some contact with human factors; for some, it’s from a design aspect, while others address it from a regulatory perspective. This session will seek to address the topic from both sides, discussing best practices for implementation, the benefits of it, and why it should matter to everyone from design team through to marketing. Join these two seasoned professionals as they have an open dialogue on topics including usability testing, formative vs. summative testing, human factors for a device used by a patient vs. a healthcare professional, and more.