Victoria Pankovich
Manager, Regulatory Services

Reporting to the Senior Director Pharmaceutical & Medical Device Consulting, Victoria Pankovich supports clients through assembling and processing FDA submissions including Drug Master Files, Abbreviated New Drug Applications and New Drug Applications. Serve as the primary US Agent for all required communications with FDA on behalf of clients, including Establishment Inspection coordination with FDA, Drug, Medical Device and Food facilities registration; Drug and Medical Device product listings; Color Certification requests; FDA Inspection Notifications; FOl and FDA Controlled Correspondence requests.