Paula Guerra

Dr. Guerra brings more than 8 years of experience in the pharmaceutical industry, working in Research and Development and Regulatory Affairs. She has managed several successful regulatory submissions to Health Canada and the United States (US) Food and Drug Administration (FDA), including Investigational New Drugs (INDs), Abbreviated New Drug Applications (ANDAs), and New Drug Applications (NDAs). Dr. Guerra has a strong understanding of quality and Good Manufacturing Practices (GMPs), which she leverages when implementing the Chemistry, Manufacturing, and Controls (CMC) strategy. In her current role as Regulatory Affairs Manager at Nutrasource, she provides scientific and regulatory support on existing projects, as well as during the evaluation of new business opportunities. Paula also actively participates on the Global Prebiotic Association’s (GPA) Scientific & Technical Committee, writing and reviewing scientific content.

Dr. Guerra holds a Ph.D. in Analytical Chemistry from the University of Barcelona. She studied emerging contaminants and their impact on the environment and humans. She is a published author of 25 peer-reviewed journal articles and two book chapters.