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DAY 2 Session 5: Device Design, User Interface, Human Factors, and Quality Format: Presentations and a Panel Discussion with Q&A (Virtual and In-Person Attendees) This session examines how device user interface differences in GLP-1 products affect substitutability, bioequivalence, and FDA expectations for Comparative analyses (CA) and Comparative Use Human Factors (CUHF) studies, and addresses device engineering and drug-device compatibility considerations that impact performance, bioequivalence, and ANDA review for GLP-1 generic combination products

GLP-1 receptor agonists are medications that mimic this hormone, amplifying and extending its effects in ways your body cannot produce on its own

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