About me
Ron Fitzmartin is a Senior Advisor in the Data Standards Branch, Office of Regulatory Operations, Center for Biologics Evaluation and Research, FDA. He provides policy and strategy consultation on electronic regulatory submissions and standardized data. Ron serves as Rapporteur for the ICH M11 Expert Working Group, Co-chair of the Global IDMP Working Group, and Chair of the IDMP Working Group under the International Pharmaceutical Regulators Programme. Prior to FDA, Ron held several leadership positions in the pharmaceutical industry. Ron received his PhD in Statistics from the University of Maryland, College Park.
