Authors: Rosie McLaughlin, Susan Banbury, and Kieran Crowley
Ever since Zydis® lyophilization technology became the first approved ODT in the U.S. in 1996, the emergence of multiple ODT technology platforms have created regulatory challenges due to increasing variance in the critical-product attributes of ODTs, notably disintegration time and tablet size. The authors, Catalent technical directors and managers, discuss the various responsive technologies available to the manufacturer as well as the recent implications of the U.S. Food and Drug Administration’s Guidance for Industry: Orally Disintegrating Tablets.