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A comprehensive global solution which integrates and reports all forms of
clinical trial information for quick, reliable and easy management.

The need to maintain focus among disparate trial sites and ensure compliance to clinical protocol requires strong internal and external communication procedures. Trial sponsors require information and accountability regarding the performance of critical trial processes; trial managers must manage resources, logistics, and effectively communicate common goals. Unfortunately, many trials are disrupted and slowed by cumbersome workflow processes and the lack of efficient coordination.

Afferenz's Acceliant Trial Management module provides a fully integrated global solution for coordinating and managing all clinical trial activities. With Acceliant Trial Management, bottlenecks and other underperforming areas within trials can be easily identified. In addition, Acceliant Trial Management's dedicated trial environment, messaging, task management, and calendaring functions facilitate real time, two-way communication during the conduct of trials.

 
Acceliant Trial Management Benefits
 
  •  Manage the development and dissemination of trial Standard Operating Procedures (SOPs)  and checklists

  •  Track trial activities from trial design to submission

  •  Track site progress during the enrollment process

  •  Collaborate with site, sponsor, and CRO personnel through dedicated messaging and  groupware

  •  Facilitate interactive physician communication through online Discussion Forum

  •  Schedule and plan meetings, manage and allocate resources

  •  Generate real-time recruitment, activity, and other standard or custom reports

  •  Track trial supplies and logistics

  •  Provide trial information and news via an online newsletter

  •  Review and address adverse and serious adverse events

  •  Track protocol violations

  •  View individual patient trial history

  •  Easily generate detailed reports, including protocol specific endpoints