Associate Principal Consultant
Mary provides quality assurance, quality management systems, compliance, and regulatory affairs support to the healthcare product industry. Her primary expertise is in quality management systems (QMS), the provision of quality oversight of CMC development activities, compliance with current Good Manufacturing Practices (cGMP), and quality control (QC). She has nearly 20 years of experience in the pharmaceutical industry and held previous roles in QC analytical testing, QA oversight, and CMC regulatory affairs for small molecule, solid-oral dosage, and oral solution/suspension products. Mary has a B.S. in Biochemistry from the University of Missouri in Columbia, Missouri.