Video

Establishing Realistic Development Timelines With A CDMO

Source: Outsourced Pharma

This segment of the Outsourced Pharma Live event, “Small Molecule Outsourcing: Getting Timelines, Tech Transfer and Analytics Right," details how sponsors can build realistic development and manufacturing timelines with CDMOs by combining complete transparency, upfront risk assessment, phase-based planning, and shared Gantt-style project dashboards instead of rushing straight from research to GMP, featuring panelist Vadim Klyushnichenko, VP Bio/Pharmaceutical Development & Quality at the Calibr-Skaggs Institute for Innovative Medicines.

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