• Introduction
  • Experience
  • Project Management
  • Quality
  • Locations
• IVRS / IWRS - IXRS
  • IXRS Features and Client Benefits
  • IXR Express
  • Dynamic Patient Randomisation and Dosing
  • Patient Tracking & Management
  • Clinical Trials Materials Management
  • Clinical Supply Management
• Reporting
  • Features
  • Suites of Reports
• ePRO
  • Why Use ePRO?
• Statistical Services
  • Dynamic Patient Randomisation & Dosing
  • Adaptive Trial Design
  • Psychometric Services for ePRO
• Web Drug Reconciliation
• Data Integration & Reporting
  • Reporting
  • Ad-hoc Reporting
• Clinical Hotline
• Technical Support

EDC – iTrial EDC

iTrial EDC™ is a user-friendly software that helps increase efficiencies within clinical trials by collecting, cleaning and reporting of trial data across sites worldwide. Clients benefit by using both Almac’s IVRS/IWRS technology and iTrial EDC, as data captured in one tool is automatically populated into the other, eliminating redundant data entry and queries. iTrial’s flexibility and user friendly interface combined with Almac’s customer service and project management help make our clients’ experience easier throughout the duration of a trial.

Almac’s iTrial EDC™ system allows clients to benefit from the following:  

• Cost Effective
• User Friendly Interface
• Speed of System Set Up
• Flexible, Mid-Study Updates
• In-House Almac 24.7.365  Global Technical Support
• Multi-lingual Capabilities

• Quick Page Turns

 Almac’s iTrial EDC™  features the following:

• Built in Integration with IXRS ™ 
• Easy-to-use interface for quick adoption
• Compatible with other eClinical solutions
• Immediate access to patient data 24.7.365
• Flexible interface allows for custom designed CRFs
• Real time reporting to track study progress
• PDF generation of eCRFs for site archival purposes
• Fast and flexible mid study updates
• Support for facilitating Adaptive trial designs
• Standard, custom, and ad-hoc reporting capabilities
• Training available via the web and / or on-site