The 3rd LNP Characterization and Analytical Development Summit is dedicated to revolutionizing your LNP drug product quality, safety, efficacy and regulatory compliance.
Topics
- Biophysical characterization to comprehend LNP in vivo and in vitro behavior
- Different characterization techniques for early- stage development to select the most robust methods: fluorescence, chromatography, imaging, and cryo-EM
- Potency assays for safety and quality assessments, employing gold standard techniques and validated assays
- Complex LNP drug products with targeting moieties and multiple payloads across oligonucleotides, CRISPR-Cas9, RNAs, and beyond
- Robustly tested critical quality attributes and release criteria for confidence in pipeline development and regulatory submission
