Begin Your Compliance Journey
Comprehensive validation and warning letter analysis to eliminate regulatory hurdles
Our team has dedicated years to developing robust validation frameworks and advanced warning letter analysis tools that ensure 100% coverage of Title 21 CFR requirements, dramatically reducing regulatory delays and compliance gaps.
Prolog-Powered Validation
Complete CFR code validation with exhaustive verification
1
Select CFR Codes
Choose relevant Title 21 CFR codes from our comprehensive database
2
Complete Forms
Fill out structured validation forms for each selected code
3
Review & Submit
Review automated validation results and generate compliance reports
Warning Letter Analysis
AI-powered analysis of FDA warning letters to identify patterns and risks
1
Upload Letters
Input FDA warning letters for analysis via URL or text
2
Pattern Analysis
Review AI-detected patterns and violation relationships
3
Risk Assessment
Get insights on potential compliance risks and recommendations
Key Platform Features
Validation Features
- Exhaustive verification of each CFR requirement
- Automated logical analysis of compliance data
- Real-time validation feedback
- Complete audit trail generation
Analysis Features
- Pattern detection across warning letters
- Risk prediction and violation relationships
- Historical trend analysis
- Automated compliance recommendations