Grant S Griffin Drsc Fraps
Managing Member, Griffin Regulatory LLC | Regulatory Policy and Intelligence | 15+ Years | Doctor of Regulatory Science (DRSc) | Fellow of the Regulatory Affairs Professionals Society (FRAPS) | Greater Chicago
- Role
- Fellow at No Patient Left Behind
- Location
- Chicago, IL, US
- LinkedIn followers
- 500 followers
About Grant S Griffin Drsc Fraps
Currently I am Managing Member at Griffin Regulatory LLC, a regulatory consultancy for the pharmaceutical and biotechnology industry. For the last 20 years, I have lived in greater Chicago and worked in healthcare. For the last 15 years, I have worked specifically in regulatory affairs at large pharmaceutical and startup biotechnology firms in virology, transplant, neuroscience, rare disease, and oncology therapeutic areas.During my tenure at AbbVie, our team obtained approval in 2017 for glecaprevir/pibrentasvir, which was prescribed to approximately patients with chronic HCV in the US between 2017 and 2019. In 2019, our team obtained approval for glecaprevir/pibrentasvir for adolescent patients, and we were nominated for an AbbVie President’s Award.In 2017, I completed a Doctor of Regulatory Science (DRSc) program at the University of Southern California (USC), and in 2023, I was recognized as a Fellow of the Regulatory Affairs Professional Society (FRAPS). As of December 2025,~60 students have completed the DRSc program, and ~180 professionals have become RAPS Fellows.
Experience
Fellow
Feb 2026 — Present · Washington, DC, US
Education
University of Colorado Law School
Mini Law School (14 Weeks)
2021 — 2022
Harvard Law School
Certificate, Law
2024 — 2024
Harvard Medical School
HMX Fundamentals - Genetics, Biochemistry, Physiology, Pharmacology, and Immunology (50 Weeks)
2021 — 2022
USC Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences
Doctor of Regulatory Science (DRSc), Regulatory Science
2012 — 2017
USC Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences
Master of Science (M.S.), Regulatory Science
2011 — 2013
University of Iowa
Bachelor of Arts, Russian (With Honors) and History (With Honors)
Skills
- Medical Devices
- Clinical Research
- U.s. Food and Drug Administration (Fda)
- Drug Development
- Regulatory Affairs
- Lifesciences
- Software Documentation
- Ctms
- Clinical Trials
- Electronic Common Technical Document (Ectd)
- Life Sciences
- Regulatory Requirements
- Protocol
- CRO
- Ectd
- Pharmaceutical Industry
- Sop
- Fda
- Regulatory Submissions
- Gmp
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