Dr. Xujin Lu is a pharmaceutical consultant. Dr. Lu has more than 30 years of experience in pharmaceutical industry for research and development. His expertise includes development of in-vitro dissolution methodologies to assess the release of drugs from innovative formulations, predicting their bio performance, and ensuring quality control for newly developed products. Dr. Lu is active members of AAPS, ACS, and SAS, and a past Chair of the In Vitro Release and Dissolution Testing (IVRDT) Focus Group of AAPS. Dr. Lu currently serves on the USP Expert Panel on New Advancements in Product Performance Testing, USP Expert Committee of Dosage Forms, and the Editorial Advisory Board of Dissolution Technologies journal.

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