Preclinical Study Management
End-to-end management of preclinical studies with automated workflows and comprehensive data integration.
Key Capabilities
40%
Faster study setup time
80%
Reduction in data errors
60%
Improvement in data reuse
100%
Audit trail compliance
What We Do
1. Commercial AI
1. Commercial AI
1. Commercial AI
Sales operations agent
Market access agent
Marketing Intelligence Agent
Market Affairs agent
Problem Addressed
Preclinical studies generate vast amounts of complex data that must be managed in compliance with GLP requirements. Manual processes lead to delays, data quality issues, and difficulty in aggregating results across studies.
Where It Fits
Bridge between Discovery Research and Clinical Development, enabling efficient translation of promising candidates into IND-ready packages.
Key Capabilities
1. Commercial AI
1. Commercial AI
1. Commercial AI
Sales operations agent
Market access agent
Marketing Intelligence Agent
Market Affairs agent
Study Protocol Management
Digital protocol design with templates, version control, and automated amendment tracking.
GLP Compliance Automation
Streamlined capture of animal study data with automated calculations and quality checks.
In Vivo Data Capture
Streamlined capture of animal study data with automated calculations and quality checks.
Histopathology Integration
Digital pathology integration with AI-assisted analysis and peer review workflows.
SEND Compliance
Automated SEND dataset generation for regulatory submissions.
Cross-Study Analytics
Meta-analysis capabilities across studies for informed go/no-go decisions.
How Clients Engage
1. Commercial AI
1. Commercial AI
1. Commercial AI
Sales operations agent
Market access agent
Marketing Intelligence Agent
Market Affairs agent
Assess
Evaluate current state and identify opportunities
1
Design
Architect solutions tailored to your needs
2
Implement
Execute with proven methodologies and best practices
3
Scale
Optimize and expand for enterprise-wide impact
4
Our Solutions
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