Priscilla M. Pastrana López U.S. FDA

Priscilla María Pastrana López is a Consumer Safety Officer in Office of Regulatory Affairs/Office of Medical Products and Tobacco Operations/Office of Biological Products Operations/Biological Products Inspectional Staff (Team Biologics). Priscilla has been with the FDA for 11 years. She started in 2011 at the Center of Biologics Evaluation and Research/Office of Compliance and Biologics Quality/Division of Manufacturing and Product Quality (CBER/OCBQ/DMPQ), where she done reviews and inspections of biological products and devices regulated by CBER. She also participated in regulatory meetings with the industry and translated non-English inspection reports submitted by other international regulatory agencies that have mutual recognition agreements with the FDA. In DMPQ, she developed the Remote Interactive Evaluation (RIE) program and conducted the first RIE in CBER. Prior joining the FDA, Priscilla worked in the private sector as a validation specialist for over nineteen years in several pharmaceutical companies in Puerto Rico and Maryland.

Priscilla has a Bachelor of Science degree in Biology with a minor in Microbiology from the University of Puerto Rico, Humacao Campus and Project Management Certification from Anne Arundel Community College. She is fluent in English, Spanish, French and German.