Carrie-lynn Langlais Furr
Vice President of Regulatory Affairs and Program M
PHARMA
AmpliPhi Biosciences corporation
Australia
Biography
Dr. Furr brings over a decade of integrated product development and regulatory affairs experience to this new position at AmpliPhi. Prior to joining the Company, Dr. Furr served as Senior Director of Operations at Rho, Inc., a clinical research organization, where she also held leadership roles in regulatory affairs, integrated product development, program management and medical writing. Dr. Furr’s prior experience includes providing strategic and operational support throughout all phases of clinical development, including formal interactions and negotiations with regulatory authorities as well as submission of several biologics license applications and new drug applications with the U.S. Food and Drug Administration. She received a Ph.D. from Texas A&M University where she studied bacteriophage lifecycle and lysis mechanisms, biochemistry, and biophysics.
Research Interest
Pharma, Clinical research, Pharmaceutical sciences
