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On 30 April 2026 (16:50 17:50) at the Oligonucleotides & Peptides Xchange, Boston, this roundtable brings together senior scientists to discuss: Detecting and quantifying variability before it impacts critical quality attributes Analytical controls across synthesis, conjugation, and purification Evolving acceptance criteria from early development through to GMP manufacturing Developing stability-indicating methods sensitive to upstream variability Integrating QC with manufacturing and supply teams to reduce deviations Led by Debasis Patra (Head of CMC Operations, OliX Pharmaceuticals, Inc.), with over 20 years of experience across process R&D, regulatory strategy, and global manufacturing scale-up

Fourth, the tirzepatide not working anymore guide addresses what happens when initial results plateau or stop, which can occur regardless of medication source