Clinical Trial Document Analysis

AI-Powered Clinical Trial Document Processing

Clinical trial documentation demands exceptional accuracy to ensure research validity and participant safety. Peslac's document intelligence system brings precision to processing complex clinical research materials.

Advanced Document Analysis

Our AI technology thoroughly examines trial documents:

• Protocol amendments
• Consent forms
• Case report forms
• Adverse event reports

The system learns from your research protocols and documentation standards, building a deep understanding of both standard and study-specific requirements.

Custom Workflow Creation

Research teams can design specialized processing workflows using Peslac's tool builder interface. This allows clinical staff to:

• Specify extraction requirements
• Implement validation rules
• Create automated notification processes based on safety parameters and study protocols

Field-Level Extraction Capabilities

Our system excels at handling complex clinical data:

• Recognizes medical terminology
• Processes measurement data
• Captures detailed observations
• Maintains accuracy with challenging elements like:
  • Laboratory results
  • Medication records
  • Adverse event descriptions

Multi-Site Document Handling

Peslac's processing engine handles documentation from multiple study sites with consistent reliability:

• Manages varying form formats
• Adapts to different submission methods
• Performs automated cross-referencing against protocol requirements
• Validates data against established parameters

Real-World Impact

Research organizations using Peslac's trial processing solution report:

• 80% faster documentation processing compared to manual methods
• Improved handling of high-volume data collection periods
• Significant improvements in data quality
• Faster identification of safety signals

Comprehensive Audit Trails

Our platform maintains detailed records of all processing activities:

• Users can review extraction results
• Make necessary adjustments
• Provide feedback to improve system understanding of documentation variations

Integration and Data Flow

• Secure APIs enable smooth integration with existing clinical trial management systems
• Processed data automatically flows into:
  • Electronic data capture systems
  • Safety monitoring platforms
  • Regulatory documentation tools

This eliminates manual data transfer and reduces the risk of transcription errors.

Scalable Performance

Peslac's solution scales effortlessly with trial complexity and size:

• Processes documentation for single-site or multi-center studies
• Handles supporting documentation and regulatory submissions
• Delivers reliable results across all study phases

Analytical Insights

Our platform provides valuable data on documentation patterns:

• Tracks processing times
• Monitors query rates
• Identifies exception patterns across study sites and visit types

This information helps optimize trial procedures and resource allocation.

Robust Security Measures

Security remains paramount throughout trial documentation processing:

• Implements strict access controls
• Maintains detailed audit logs
• Ensures all handling follows GCP guidelines and regulatory requirements

Peslac's intelligent document processing for clinical trials offers tangible improvements in efficiency and accuracy. By combining AI-driven extraction with user-defined rules, we provide unmatched flexibility in managing complex research documentation.