Table of Contents

1. Improved Compliance

  • Strengthened sponsor oversight: Enables sponsors to demonstrate evidence of study oversight in compliance with evolving regulatory guidelines.

2. Automated CTMS Data Transfer

  • Streamlined data practices: Minimize manual data entry, eliminate redundant processes, reduce errors, and ensure data consistency.
  • Optimized resources: Reallocate time spent on building custom reports and reconciling data to support more strategic initiatives.

3. Enhanced Collaboration

  • Shared view of critical data: Foster transparency and proactive communication between Sponsor and CRO.
  • Faster issue resolution: Identify and address challenges together quickly and efficiently.
  • Informed decision-making: Leverage real-time data for better insights.

4. Accelerated Timelines

  • Faster study start-up: Initiate trials more rapidly and gain real-time visibility into trial progress.
  • Rapid delivery of results: Accelerate the path to discovery and patient benefit.

5. Focused Strategic Activities

  • Drive innovation: Empower your team to focus on data analysis, patient engagement, and scientific breakthroughs.
  • Minimize technical debt: Drastically limit custom tech integrations, including ongoing maintenance, and focus on strategic technology projects.

To learn about activating this native feature within Veeva CTMS contact us today to schedule a meeting.