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Target e*CRF® + e*Studio®

EDC Solution for Sponsors and CROs of all sizes and types

Target e*CRF® + Target e*Studio® is a cloud-based EDC software that enables CROs, pharmaceutical, and device companies to design, test, and deploy their studies globally. It enables the user to capture, manage, and report clinical trial data electronically.

  • Target e*CRF Application - Design the perfect study for your clinical needs
  • Target e*CTR Viewer - Direct Data Entry Capability
  • 21 CFR Part 11 - Compliant with federal mandate for electronic record systems
  • Customizable Case Report Form and Edit Check
  • Electronic Informed Consent (Target e*ICF™) - Collect patient registration and consent online
  • ePRO (Mobile App) - Data entry by patient
  • IRT - Randomization and IMP Management
  • External Data Integration

Flexible and Reliable with All the Features CRO Needs

Features Target e*CRF
+ Target e*Studio
Accessibility and visibility by Role
Accessibility and visibility by User
Subject Multiple Locks
Communication between Roles
Data Exporting to Extension Study
Central and Local Lab
Notification from the system
Protocol Deviation
Medical Coding
SAE Handling (Target e*Pharmacovigilance)
Remote SVD (File upload/download)
Randomization
Unblinding
IMP
ePRO
eIC (Target e*ICF™)
Monitoring Report
Data transfer to third party system
Data Export (CSV, Excel, Text and SAS Dataset)
Average Implementation Time < 3 Months
Average Required User Training 1 - 2 Hours