Jessica Douglas
Consultant
Jessica Douglas provides regulatory chemistry, manufacturing, and controls (CMC) and compliance support to the pharmaceutical products industry. She is experienced in authoring, reviewing, and publishing CMC sections of Investigational New Drug Applications (INDs), Investigational Medicinal Product Dossiers (IMPDs), and New Drug Applications (NDAs). Additionally, she prepares, publishes, and performs data accuracy reviews of electronic regulatory submissions to Health Authorities. Prior to joining SciLucent, Jessica worked as a Regulatory CMC Technical Writer where she authored and reviewed CMC submissions. Jessica has a B.S. in Animal Sciences from the University of Missouri-Columbia.
