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Presentation: Using CDISC Standards to Optimize End-to-End Clinical Trials

iMedNet User Group, October 2015

CEO Mark Wheeldon travelled to Minneapolis, MN in October 2015 to deliver a presentation focusing on optimizing end-to-end clinical trials using CDISC standards.

Mark firmly believes the future of clinical data management and regulatory review lies in the successful implementation of data standards and technologies. He highlights this thinking and the reasons behind it in this presentation.

Learning points include:

  • Business benefits of CDISC standards
  • Creating perfect libraries and encouraging reuse across trials
  • Tips to streamline study specification
  • End-to-end trial automation
  • Optimizing Study Conduct processes

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