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WHO SHOULD ATTEND?
- Health Care- and R&D Professionals in the areas of Electronic Document Management, IT and Process Innovation
- Clinical Operations and Regulatory Affairs that want to excel in their day-to-day work
- R&D Quality Leads, as well as Trial Managers and Drug Programme Leads & Clinical and Regulatory Project Managers that need to get an overview of the latest gold standards in R&D Operational Excellence to set the standards for high-performing cross functional drug development teams
- New Technical Solution Vendors
