Chase Tarnstrom

Senior Consultant

Chase is a senior regulatory affairs consultant with 3+ years of experience consulting within the Food and Drug Administration (FDA) to support successful review of submissions from regulatory divisions of market-leading pharmaceutical companies. He also worked directly for Pharma clients, using his inside knowledge of the FDA to provide strategic direction for real-world evidence utilization and approval facilitation of NDA, BLA, and 510K submissions. He is known for his strong work ethic, effective communication, collaborative approach, and commitment to staying updated with industry trends. Chase has a proven track record achieving goals for organizations navigating regulatory compliance within the pharmaceutical sector.

Academic & Professional Qualifications:
  • B.S. Public Health Pre-Clinical, Liberty University
Training, Quality Systems, & Specialties:
  • Regulatory Strategy
  • Real World Evidence
  • Risk Management
  • Post Market Requirements
  • 21 CFR, ISO, & GCP Standards