It integrates various activities and processes into a single, easy-to-use application, helping to eliminate costly delays and improve operational efficiency.

Key Features

• Centralized Study Start-Up Management:
  • Feasibility and Site Selection: Manages the feasibility, qualification, and activation of research sites. Feasibility surveys are sent to sites, which are then scored based on their responses. Selected sites are routed into the activation process.
  • Site Activation: Drives site activation through standard tasks and milestones, controlled by country-specific templates that specify required processes and documentation.
• Visibility and Tracking:
  • Dashboard Views: Provides complete visibility of start-up progress and timelines through dashboard views, allowing users to track the status of various activities.
  • Critical Path Management: Identifies and prioritizes dependent and at-risk tasks, documents, and milestones through automated critical path management.
• Efficiency and Automation:
  • Automated Processes: Automates the collection and tracking of key documents, reducing manual effort and increasing accuracy.
  • Milestone Templates: Uses milestone templates to create consistent study plans across trials, ensuring compliance with country-specific business practices.
• Collaboration and Communication:
  • Seamless Information Exchange: Facilitates greater alignment across study partners through the seamless exchange of trial information, driving better decisions.
  • Remote Access: Enables remote monitoring and collaboration between sponsors, CROs, and sites.
• Compliance and Reporting:
  • Regulatory Compliance: Ensures that all documentation processes comply with regulatory requirements.
  • Comprehensive Reporting: Offers robust reporting capabilities to track document status, monitor compliance, and generate necessary reports for audits.

Benefits

• Faster Site Activation: Reduces the time to activate sites by streamlining site selection, feasibility, ethics committee approvals, and site contract management.
• Improved Operational Efficiency: Decreases the cycle time from start-up packet sent to site activation, and from protocol approval to first subject enrolled.
• Enhanced Decision-Making: Provides insights to prioritize tasks and manage dependencies, improving overall decision-making.
• Better Collaboration: Enhances collaboration between sponsors, CROs, and sites, ensuring transparency and alignment throughout the study start-up process.