OpenText Core for Quality Management
OpenText Core for Quality Management brings simplicity to CAPA management
Production & Process Controls and CAPA
- 30% most frequently observed & cited by FDA
Most common pitfalls
- Root cause determination
- Reliable metrics documentation
Life Sciences companies report that nearly half of their quality processes are manual, which can be inefficient and error-prone and lead to increased risk of regulatory agency observations and manufacturing delays. When adverse events occur, organizations struggle to correctly isolate root causes. This is compounded by poor or nonexistent connections between systems, often from different vendors making them difficult to navigate.
OpenText™ Core for Quality Management delivers an intuitive, streamlined, and tailored user experience for completing nonconformance and corrective and preventive action (CAPA) tasks, making complex processes simple and efficient. The application ensures readiness for regulatory inspection with on-demand records, detailed reports and audit trails, reducing risk by eliminating manual quality processes.
Core for Quality Management natively integrates with OpenText content management systems, with no additional software installation or hardware investment, to ensure a single, authoritative source for regulated content across the extended organization. As a multi-tenant Software-as-a-Service application hosted in the OpenText Cloud, Core for Quality Management lowers the total cost of ownership by reducing validation and maintenance costs.
- Intuitive, modern, experience with at-a-glance layout
- Embedded root cause analysis tools and insightful quality metrics
- Seamless Documentum integration with CAPA processes
- Qualified cloud deployment