Associate Director, RIM
Zimmer Biomet
Experienced Associate Director in Regulatory Information Management (RIM) with a demonstrated history of working in the pharmaceutical and the medical device industries. Skilled in Global RIM systems deployment, Global Labeling, Document management, and Regulatory Affairs. Experience in leading cross functional teams and strong information technology professional with a M.S. focused in Informatics from Indiana University.
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Sponsored Presentation: Improve Time to Value with Integrated Product and Regulatory Data
Wednesday, October 4, 2023
11:15 AM – 11:40 AM EDT