Kristina M. Adams, PhD U.S. FDA

Kristina Adams is a Drug Product Quality Assessor whose duties include assessment of quality and controls of ANDAs, including large volume parenteral (LVP) IV bags and pre-filled syringes. She also has experience addressing controlled correspondences, advising industry on the adequacy of proposals on the CMC aspects of their ANDA submissions. Prior to joining the FDA, Dr. Adams held roles in synthesis and purification of polymers for biomedical and pharmaceutical applications. She has publications in various peer reviewed journals including Biomaterials and Pharmaceutical Technology. Dr. Adams holds a Ph.D. in Pharmaceutics and Pharmaceutical Chemistry and a BS in Chemistry; both are from the University of Utah.