Chris le PageAssociate Director CMC Regulatory Affairs at UCBSpeaker
Profile
Chris Le Page is a biopharmaceutical professional with 20 years of experience spanning process development and CMC regulatory affairs, supporting global products from early‑stage development through post‑approval.
Agenda Sessions
[BioPhorum Case Study] Structured Data for Regulatory CMC – Enabling Agile, Harmonized Submissions Through Digital Transformation
, 09:00View Session
