[ FROM MANUAL TO DIGITAL ]
Addressing Key Validation Challenges
Our client, a leading pharmaceutical company, faced significant challenges with their manual validation processes. They sought a robust software solution to drive a digital transformation, moving away from error-prone manual Computer System Validation (CSV) to a streamlined paperless validation approach. Specifically, they aimed to:
- Eliminate manual errors during testing, ensuring data integrity and accuracy.
- Streamline review and approval processes, reducing bottlenecks and accelerating validation timelines.
- Reduce validation and approval process timelines, improving time-to-market.
- Improve operational efficiency across their validation lifecycle.
- Automate test protocol execution, deviation recording, traceability matrix generation and Validation Summary Report creation.
By implementing a comprehensive digital validation solution, they aimed to achieve enhanced GxP compliance and significantly improve their overall validation workflow.
