Tara Morgen

Tara provides chemistry, manufacturing, and controls (CMC) and regulatory support to the healthcare product industry.  She also provides clinical supply and materials management support for clinical programs.  She assists in authoring CMC sections of Investigational New Drug Applications (INDs), Investigational Medicinal Product Dossiers (IMPDs), and New Drug Applications (NDAs).  Tara also assists in authoring Standard Operating Procedures (SOPs) and building out Quality Management Systems (QMS).  Tara has a B.S. in Chemistry, with a Specialization in Biochemistry from the University of Virginia.