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Session 6: Oral Semaglutide: Bioequivalence, Regulatory Considerations, and Oral Peptide Delivery Format: Presentations and a Panel Discussion with Q&A (Virtual and In-Person Attendees) This session addresses the regulatory and scientific challenges of developing generic oral semaglutide tablets, drawing on FDAs experience with PSG development and generic application review

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[PMID: 38371020] PubMed record related to this compound for laboratory literature review

Trends and disparities in technology use and glycemic control in type 1 diabetes