Isabella Rossi
Consultant
Isabella provides chemistry, manufacturing, and controls (CMC), quality and regulatory support to the healthcare products industry. She assists in authoring CMC sections of New Drug Applications (NDAs), Investigational Medicinal Product Dossiers (IMPDs) and Investigational New Drug Applications (INDs). Isabella also assists in authoring Standard Operating Procedures (SOPs) and building out Quality Management Systems (QMS). Prior to joining SciLucent, Isabella interned at the United States Pharmacopeia where she ensured harmonization of compendial excipients across all leading pharmacopeias. Isabella has a B.S. in Biochemistry from the University of Maryland.