Elaine Liong

Elaine Liong has 13 years of pharmaceutical industry experience, managing and directing regulatory intelligence and efforts from pre-IND to postmarking regulatory filings. She has written and contributed to 3 pre-INDs, 8 INDs & 1 NDA. Elaine leverages scientific and technical data with the requirements for regulatory approval, identifying and implementing regulatory strategies to innovatively advance drug discovery and development programs.