Snehal Trivedi

Associate - Washington, D.C.

Contact Information

Snehal Trivedi focuses her practice on U.S. Food and Drug Administration (FDA) policy and regulatory matters and advises food manufacturers and pharmaceutical clients in preparing FDA correspondences and other post-market filings. She draws upon 10 years of pharmaceutical industry experience and has drafted and negotiated various license, distribution, and clinical trial agreements on behalf of leading pharmaceutical companies, contract research organizations and university hospitals. Snehal has experience in facilitating due diligence efforts related to state boards of pharmacy laws and regulations related to prescription drugs and controlled substances.


  • Campbell Law School, J.D., 2015
  • University of the Sciences in Philadelphia, Pharm.D., 2000


English, Gujarati, Hindi

Professional Experience

Prior to joining Foley Hoag, Snehal was an attorney at K&L Gates in the FDA/Healthcare practice group. She is also a pharmacist licensed in New Jersey and North Carolina. 
  • “Generic Drug Submissions” chapter, Fundamentals of U.S. Regulatory Affairs, 10th Ed.
  • Ferring Pharmaceuticals, Inc. v. Burwell,” Food, Drug and Law Institute, Top Food and Drug Cases for 2016 and Cases to Watch 2017
  • “Enhancing Clinical Trial Transparency: Will the HHS Final Rule and NIH Policy Be Enough?,” American Health Lawyers Association
  • Amgen v. Sandoz,” Food, Drug, and Law Institute, Top Food and Drug Cases for 2015 and Cases to Watch 2016

Foley Hoag Alerts & Updates


  • Sutherland Cup National Moot Court Competition, Semi-finalist


  • Food, Drug and Law Institute
  • Regulatory Affairs Professional Society (RAPS)


  • “Overview of U.S. Food Law and Regulation,” Food, Drug, and Law Institute
  • “Overview of Medical Devices,” North Carolina College of Textiles
Add to Bio Folder

Download Bio

Bar Admissions

  • North Carolina