BioClinica CTMS

BioClinica CTMS

The CTMS solution offers centralized access to all clinical trial and logistical project information, streamlining study management for sponsors and CROs. Its integrated eTMF securely stores and tracks documents while ensuring compliance. With flexibility in user pricing and a rapid setup time of 2-3 weeks, it scales efficiently with project needs.

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Top BioClinica CTMS Features

  • Centralized trial data management
  • Integrated electronic trial master file
  • Scalable system architecture
  • Compliance tracking features
  • Document storage security
  • Customizable user configurations
  • Rapid startup implementation
  • Cost-effective pricing model
  • Active study usage tracking
  • Real-time project oversight
  • User-friendly interface design
  • Role-based access controls
  • Comprehensive reporting tools
  • Automated compliance alerts
  • Seamless third-party integration
  • Audit trail capabilities
  • Multi-site project coordination
  • Advanced data analytics
  • Efficient resource allocation
  • Support for global trials.