Emilee Stanczyk
Seeking Young Perspectives: Usability Testing with Children
Join us and learn our most effective tips for planning and executing usability tests with pediatric and adolescent participants.
人因工程在學名藥-器材組合產品中的應用
本次研討會適用於任何類型的擬申報仿製產品，包括但不限於預填充式注射器、筆型注射器、自動注射器、皮膚貼布和吸入器等。
Design Changes after HF Validation: How to Assess a Change's Impact and Need for Supplemental Testing
Learn how to evaluate design changes after HF validation and when additional testing may be necessary to meet usability and regulatory expectations.
PDA Conference 2025
Heading to the Parental Drug Association Conference in Vienna, Austria? Don’t miss the chance to connect with Emergo by UL’s Human Factors Research & Design team.
Swiss Medtech Expo 2025
Join Emergo by UL at Swiss Medtech Expo to explore regulatory, human factors engineering and market access strategies for innovative medical devices.
5 Methods for Evaluating Your Instructions for Use: Benefits and Drawbacks
We provide five methods to evaluate instructions for use.
Early Design Evaluations for Medical Devices
Emergo by UL helps medical device developers optimize early-stage design with expert critiques, user walkthroughs and human factors evaluations.
Human Factors Engineering Consulting for Medical Devices
Discover how human factors engineering consulting services from Emergo by UL support medical device development through expert guidance, training, and regulatory strategy.
Is Institutional Review Board (IRB) Approval Necessary for Usability Tests?
Learn when and why IRB approval is necessary for usability tests in medical device development, including regulatory requirements and risk considerations.