Salette Martinez
Associate Director - Analytical Development nChroma Bio
Seminars
Wednesday 25th February 2026
Ensuring Phase-Appropriate Method Readiness from AD Through QC to GMP
6:00 pm
- How to establish phase-appropriate analytical methods that meet regulatory expectations despite limited resources and compressed development timelines.
- Strategies to adapt and validate assays for QC environments while maintaining analytical precision and CMC consistency.
- Approaches to coordinate cross-functional transfer from development to GMP to secure compliance and minimize rework at scale.
