Pernell Abrantes

Pernell Abrantes is an accomplished professional in regulatory affairs with extensive experience in the medical device industry. Former roles include Director of Regulatory Affairs at ICU Medical, Global Regulatory Affairs Manager for Medical Devices at Pfizer, and Global Regulatory Affairs Manager at Hospira. Additional positions include Product Regulatory Affairs Leader and U.S. Regulatory Affairs Leader - Post Market at GE Healthcare, as well as Product Surveillance Quality Associate II at Baxter Healthcare. Pernell holds a Master of Science in Quality Assurance and Regulatory Science from Northwestern University and a Bachelor of Science in Bioengineering from the University of Illinois Urbana-Champaign.