Tara Morgen
Consultant
Tara Morgen provides chemistry, manufacturing, and controls (CMC), quality, and regulatory support to the healthcare product industry. She is experienced in CMC project management and clinical supply management for programs in clinical development. Tara supports the authorship, submission, and lifecycle management of United States (U.S.), European, and Canadian regulatory applications. She also assists with implementing Quality Management Systems (QMS) and authoring Standard Operating Procedures (SOPs). Tara has a B.S. in Chemistry, with a Specialization in Biochemistry from the University of Virginia.
