Qualsys’s software is used by laboratories to plan, manage and record the quality and integrity of their studies. Pharmaceuticals, agrochemicals, industrial chemical, good and cosmetics companies benefit from the software for:
- Planning and managing all processes and policies
- Collaboration and communication
- Reducing compliance burden
Assign roles and responsibilities
Use notifications and workflows to assign roles and responsibilities to individuals such as those for the study director, or groups such as those involved in the laboratory.
Manage employee competency
Manage competency and systematically maintain training records using the Training Record Manager module.
Manage any type of audit, for example study based inspections, facility based inspections and process based inspections, and record the results and follow-up activity.
Demonstrate good governance
The system provides a central system for leadership to see dashboards, visual displays and data reports for a complete picture of the health of the business.
Manage documentation such as the study plan and final report in Document Manager. Version control, audit trails and electronic signatures make demonstrating compliance natural and easy.
Qualsys supports you throughout the entire computer system validation process.
Read how Qualsys helps you to manage your entire validation masterplan, from developing your User Requirements Specification to establishing an efficient process for re-validating your system when your business processes change.
Discover how the requirements of GLP can be applied in each of Qualsys’s software modules.