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.