

Label Intelligence, formerly known as DocLabel, is the industry-leading solution for prior precedent research, competitive comparisons, and proactive tracking, generating a 6:1 return-on-investment.
Stay focused on important strategic work and rapidly, confidently answer questions from internal and external stakeholders.

Comparison
Create side-by-side tables for competitive labels and highlight changes between label versions

Automated Tracking
Stay on top of competition with automated monitoring
Safety Surveillance
Leverage AI-powered adverse event comparisons
Approved Labels from
 Food and Drug Administration (FDA) Food and Drug Administration (FDA)
 Health Canada Health Canada
 European Medicines Agency European Medicines Agency
 Medicines and Healthcare Products Regulatory Agency (MHRA) of the UK Medicines and Healthcare Products Regulatory Agency (MHRA) of the UK
 Ministry of Solidarity and Health of France Ministry of Solidarity and Health of France
- Swissmedic of Switzerland 
- Health Products Regulatory Authority (HPRA) of Ireland 
 Therapeutic Goods Administration (TGA) of Australia Therapeutic Goods Administration (TGA) of Australia
 Pharmaceuticals and Medical Devices Agency (PMDA) of Japan Pharmaceuticals and Medical Devices Agency (PMDA) of Japan
- Agência Nacional de Vigilância Sanitária (ANVISA) of Brazil 
- New Zealand Medicines and Medical Devices Safety Authority (MEDSAFE) - (Coming Soon) 
 Italy Agenzia Italiana del Farmaco (AIFA) -(Coming Soon) Italy Agenzia Italiana del Farmaco (AIFA) -(Coming Soon)
Testimonials
“saves me hours and hours of time”
      
      
      
        
        Senior Director, Regulatory Affairs, Mid-market Pharmaceutical Company
        
      
    
  “…crucial in comparison of competitor labeling”
      
      
      
        
        Associate Director, Regulatory Labeling, Mid-market Pharmaceutical Company
        
      
    
  “I defined a search, and within seconds, found an example that had not been identified by a colleague who searched for a couple days.”
      
      
      
        
        Associate Director, Regulatory Affairs, Top-tier Pharmaceutical Company
        
      
    
  “What took more than a couple of hours to complete now took less than 30 minutes.”
      
      
      
        
        Director, Regulatory Affairs, Top-tier Pharmaceutical Company
        
      
    
  "Very useful when comparing safety profiles of competitive or companion drugs."
      
      
      
        
        Senior Safety Scientist, Mid-market Biotechnology Company
        
      
    
  