Tara Morgen
Consultant
Tara Morgen provides chemistry, manufacturing, and controls (CMC) and regulatory support to the healthcare product industry. She assists in authoring CMC sections of Standard Operating Procedures (SOPs), as well as New Drug Applications (NDAs) and Investigational New Drug Applications (INDs) for submission. Tara also prepares, publishes, and performs quality control reviews of electronic submissions. Tara has been a B.S. in Chemistry with a specialization in Biochemistry from the University of Virginia and has been a member of the SciLucent team since 2020.
