Customer Success Stories
Real-world results from leading companies in regulated industries
Regeneron Cuts Deviation Closure Time by 43%
"FieldGuardian™ has transformed our compliance documentation process. Our quality team now spends less time on documentation rework and more time on critical investigations."
After implementing FieldGuardian™'s compliance overlay, Regeneron saw immediate improvements in their deviation management process:
- Reduced cycle time for processing deviation records
- Increased first-pass compliance rate from 63% to 91%
- Improved consistency across multiple manufacturing sites
- Enhanced auditability of compliance documentation
Takeda Avoids Potential 483 with AI-Powered Compliance Review
"The FieldGuardian™ overlay flagged an incomplete CAPA root cause analysis just 12 hours before submission to our regulatory affairs team. This potentially saved us from a serious finding in our upcoming inspection."
Takeda's quality management team reported significant benefits from their implementation:
- Identified critical gaps in root cause analysis documentation
- Provided specific improvements aligned with regulatory expectations
- Reduced investigation reopening rate by 58%
- Streamlined compliance checks without burdening IT resources
Abbott Reduces QA Overtime by 310 Hours Per Site
"Our QA specialists were routinely working overtime to complete documentation review cycles. FieldGuardian™ has dramatically reduced these review cycles, resulting in significant time and cost savings while improving employee satisfaction."
Abbott's implementation across multiple manufacturing sites yielded consistent results:
- Standardized compliance language across global operations
- Reduced QA specialist burnout by minimizing documentation rework
- Accelerated training of new QA personnel
- Decreased time to close compliance documentation by 37%
What Our Customers Say
Feedback from quality professionals using FieldGuardian™ daily
Proven Results Across the Industry
Average performance improvements reported by customers
Reduction in Documentation Rework
Decrease in the number of revision cycles needed before final approval
Improved First-Pass Compliance
Increase in quality documents approved without any revisions required
Return on Investment
Average ROI reported by mid-size biotech companies (500-1000 employees)
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