Better Trials, Better Outcomes:
Why Every Biopharma Needs a CTMS

Managing the growing complexity and cost of clinical trials requires strong operational controls. A robust clinical trial management system (CTMS) delivers this control across both insourced and outsourced study models, streamlining operations to accelerate trial completion and regulatory submission.

This comprehensive guide will explore how a CTMS can help you take control of your trials regardless of your operating model. We’ll dive into the challenges of managing clinical trials without a centralized system and share how a CTMS:

  • Improves efficiency and reduces errors with automated workflows and centralized data management
  • Fosters seamless communication and data sharing between internal teams and CROs
  • Improves study oversight to lower risks of data quality problems and serious compliance gaps
  • Enables data-driven decision-making with comprehensive reporting and analytics

What is your clinical trial operating model?

My team outsources
most clinical trial
activities to a CRO.

My team performs most
clinical trial activities
in-house.