Oncology
For years, Sara worked in a hospital, making care possible for others. Now, after being diagnosed with breast cancer, she was the one in need of care.
As an expert regulatory strategist, Pengfei provides strategic regulatory, technical, and clinical pharmacology drug development support across all phases of product development. A former FDA clinical pharmacology team leader, he leverages over 18 years of regulatory experience to expedite trial designs, dose selection and optimization, and clinical pharmacology approaches for pediatric and rare disease therapy development. Former roles also include VP, Global Head of Clinical Pharmacology at I-Mab Biopharma and Clinical Pharmacokineticist at ArQule.
Education
Pengfei earned his PhD in Pharmaceutical Science from the University of Tennessee Health Science Center, and an MS and BE in Biopharmaceutics from China Pharmaceutical University.