GMP Manufacturing Workflows

Case Study

Digital Quality Process Prevents Erroneous Releases and Avoids High-Risk Deviations

Explore ways to achieve cost savings and practice cost avoidance. Adhere to Good Manufacturing Practice (GMP) standards with the help of ProcessX.

Manufacturing plants are still largely paper-based. Unfortunately, manual processes contribute to Good Documentation Practice (GDP) errors and lengthy deviations. And the expenses add up fast. Deviations range from $5,000 to $15,000 each, and corrective and preventive actions (CAPAs) range from $5,000 to $20,000 each. When it takes up to 90 days to resolve these issues, they really slow down your processes.

The potential cost savings with ProcessX is substantial. Besides decreasing the number of deviations, CAPAs, and GDP errors, ProcessX helps your life sciences organization:

Deviation cost avoidance
Mitigate re-runs and batch or lot losses
Reduce the risk of recalls
Shorten cycle times
Decrease storage costs
Increase audit response times

See how ProcessX saved 2,100 hours of manual work per year at 32 sites, which equates to 67,200 hours saved. By reducing high-risk deviations like erroneous releases, the multi-national pharmaceutical company improved its compliance and release cycle time.

Commit to Go Paperless

ProcessX GMP workflows digitally transform paper-based processes and records to help ensure your organization achieve and maintain compliance. They may even inspire your facility to be a factory of the future. After all, digital transformation and paperless validation systems are commendable goals in the life sciences industry. Advantages of paperless manufacturing include:

Minimizing—or eliminating—hard-copy documentation
Making documents available where and when they’re needed
Improving the accuracy of documentation
Tracking changes to documentation
Ensuring regulatory compliance