Catherine Gambert is a Senior Consultant, Regulatory Affairs and Regulatory Information Systems, at ProductLife Group, providing expertise in regulatory information management (RIM) strategies, Extended Eudravigilance Medicinal Product Dictionary (XEVMD) and Identification of Medicinal Products (IDMP) standards.
Drawing on her proven expertise in project management across regulatory affairs and in advancing processes across research and discovery, Catherine provides consultation on comprehensive RIM systems configuration and implementation strategies for migrating legacy databases into regulatory information systems. She has overseen a major RIM project for a large pharmaceutical company, defining the scope across the product portfolio and implementing a data governance and supporting data quality framework for the RIM system.
Before joining ProductLife Group, Catherine was Director of Regulatory Informatics and Submission Management at Merck Serono. She is a Chemistry Engineer and has a master’s in Analytical Chemistry from the University of Lyon.