Drug and device accountability is a critical regulatory requirement, but it can be complex and time-consuming especially when done on paper. Often, there are also expensive equipment and supplies to manage and track. To help lower the cost of clinical trials, Sponsors and CROs need an electronic product accountability system that integrates with their Clinical Trial Management System (CTMS).

Merge CTMS & EDC, formerly StudyManager Evolve, product accountability feature allows you to easily track medical devices, study drugs, equipment, and other clinical trial materials.

Product Accountability Features

• Full inventory logging, including records
  of serial numbers and lot numbers
• Tracking of distributions made to sites
• Electronic signature for shipments received
• Allows for site initiation of returns
• Track any item down to the study subject
  to which it was assigned
• Embedded reports for quickly viewing
  in-house and site inventory

Learn more about Merge CTMS & EDC features »