Kevin Amiri

Kevin Amiri, PhD, RAC, is an experienced regulatory affairs consultant with a robust background in managing CMC regulatory changes and developing filing strategies across various industries, including pharmaceuticals, biotech, and medical devices. Since May 2016, Kevin has held the position of Senior Regulatory Affairs Consultant at PAREXEL while simultaneously providing regulatory consulting services at Validant and Pharmabiodevice since 2015. Kevin also has experience with Pharmalink Consulting, Sanofi, Pfizer, Quintiles, Merck, and Regeneron, focusing on post-approval filing strategies, QA oversight, and regulatory compliance. Kevin earned a Doctor of Philosophy (PhD) in Food Science and Technology from the University of Tennessee, Knoxville.