We will demonstrate how to:

  • Ensure compliance with standards and quickly react to change in regulatory environment;
  • Simplify your audit process, easily report issues and ensure corrective actions (CAPA) tracking;
  • Implement a total quality management system enforcing SOPs and ensuring document control easily across your organization.


In a broader way, you will learn how to:

  • Implement quality measures to every department with no recurring IT intervention and make sure your company is compliant at all levels;
  • Gain insights on activities in all departments and improve visibility on data of all kind;
  • Eliminate slow paper-based quality processes while remaining compliant to strict FDA and ISO standards and regulations;
  • Optimize time spent on repetitive tasks, IT maintenance and complexe configuration.

40 min

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