Judith Ford, M.S.

Judith Ford, M.S. has a diverse work experience in the field of Regulatory Affairs. Judith started their career in 1999 as an Analytical Chemist and QC Technician at Chattem Chemicals, Inc. In 2001, they were promoted to Validation Chemist at the same company. In 2010, they were promoted again to Manager - Regulatory Affairs at Chattem Chemicals, Inc. In 2015, they moved to Olin Chlor Alkali Products as a Quality and Environmental Specialist, where they managed the ISO 9001 Quality Management System and the Responsible Care 14001 EHS&S Management System. In 2017, they moved to Crown Laboratories, Inc. as a Regulatory Affairs Specialist, where they were responsible for ANDA submission preparation and life-cycle maintenance, drug adverse event reporting, and drug listing preparation and submission. In 2018, they moved to Summit Biosciences Inc. as Manager of Regulatory Affairs.

Judith Ford, M.S. earned a Bachelor of Science (BS) in Chemistry from The University of Tennessee at Chattanooga. Judith then went on to receive a Master of Science (MS) in Regulatory Science from the University of Maryland School of Pharmacy in 2016.