
Nate Edwards of Arya Consulting moderates a discussion with Elisabeth Gardiner of Tevard Biosciences and Donny Xu of the RTW Institute about the regulatory and manufacturing hurdles facing rare disease drug developers.
Discover how Avantor’s global innovation centers help biopharma teams shorten timelines through expert-guided resin and buffer selection, downstream process development optimization, hands-on support and real-world application data. Includes a case study on faster clinical trial readiness.






