Naiqi Ya is a Team Leader in the Divison of Chemistry II, Office of Generic Drugs, Center for Drug Evaluation and Research, FDA. In his current capacity, he is responsible for reviewing chemistry and manufacturing control sections of new drug applications (ANDA/IND/NDA). Prior to joining FDA in 1996, he held
a position at Biocraft Laboratories, Inc., where his responsibilities included developing and validating analytical methods for drug substances and drug products. He received his Ph.D. in Bioanalytical and Biophysical Chemistry from New York University in 1994.
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