>> CUSTOMER LOGIN TRIALVISION—Online Document Management
Managing the Clinical Trial Document Production Process
ICD Global's Document Services are powered by TrialVision, which enables us to take the CRF process to a whole new level, where the intelligence you need is at your fingertips. So the status of your project is never a mystery, or an impediment to your clinical trials process.
At-a-Glance Calendar
Provides a quick status of the day’s activity, while allowing drill-down access to individual events.Order Review
Allows for a complete review of each active CRF component order.Site Address Control
Allows the manager to coordinate the entry of site information for the study.Shipping Tracking
Enables online tracking of the number of boxes shipped, contents of boxes, and the study coordinator designated on the packing slip.Project File Upload
Uploads all design files and project files via a secure connection.Inventory
Maintains a complete online inventory of any finished study material for future delivery.Reorder
Allows for online reordering of any study component.Accounting
Stores all accounts receivable and payable information in a secure site for fast online review.Reporting
Generates custom reports on demand.Threaded Discussion/Notes
Records time-sensitive notes and discussion points for each component.Event Notification
Automatically notifies stakeholders of all milestones and events via email.Intuitive Interface
All critical data is only one click away.
“TrialVision saves me many hours each week. In fact, I take this system so much for granted, I can't guess how many hours of phone calls, paperwork and filing it saves.”
“The software was easy to use. The interface between TrialVision and Adobe Acrobat was seamless... technical support was very helpful and responded quickly...the software has flexibility for customization...”
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