As the Senior Regulatory Affairs Director for Business & Technology Transformation, Donald works with the Regulatory Affairs and Drug Development Solutions (RADDS) team at IQVIA to add and update technology solutions to RADDS's business processes. His experience bridges the business and technology divide that spans Regulatory submissions, document management, and Regulatory Information Management, especially as they integrate with other departments and systems. Having worked in several organizations of different sizes, he provides perspectives from sponsors, vendors and now CROs. He is a strong proponent of standards and data governance.

Managing Director, Marr Consultancy Ltd. Recognised expert in IDMP through work in ISO, EU IDMP Task Force, Conference Speaker and numberous engagements with top 25 pharma (and other pharma clients), software houses and service providers in the e-Regulatory space.

Andrew has been in biotech since 2002, serving first in Quality Assurance positions and subsequently as a Regulatory Operations professional. He has led the Vertex publishing group for almost 7 years and has led successful marketing application for three products in the past four years in the US, Canada and EU. In addition to heading up the publishing team, Andrew has worked on the deployment and validation of two publishing systems and recently, a complete overhaul of the information management system.