Frank Viscomi

Frank Viscomi is an experienced professional in CMC Regulatory Affairs, currently serving as Director at Eisai US since September 2018, where responsibilities include developing regulatory strategies for global CMC submissions, resolving regulatory issues, and collaborating with various internal teams to ensure compliance. Prior to Eisai, Frank worked at Synthon Pharmaceuticals as a Regulatory Affairs Specialist, preparing and submitting FDA-required documents for generic drug products. Frank's career began in 1983 at Pfizer as a Formulator for solid dosage forms, followed by a significant tenure at GSK as a Pharmaceutical Development Scientist, focusing on drug candidate properties and formulation development. Frank holds a Bachelor's degree in Pharmacy from the University of the Sciences in Philadelphia and further education from the University of Wisconsin-Madison.