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eScreening Subject Information Management

Trial participant identity verification and closed-loop enrollment management with biometric authentication and real-time risk alerts.

Solution by Taimei Technology
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Overview

eScreening is a Trial Participants Information Management System developed by Taimei Technology, designed to support secure enrollment and high-quality recruitment in clinical trials. The platform provides a comprehensive suite of tools for managing trial participant data, verifying identities, and maintaining closed-loop oversight throughout the entire trial lifecycle.

eScreening is built for clinical research sites and organizations that require rigorous participant management, risk mitigation, and regulatory compliance. By combining advanced identity verification with data-driven risk alerts and a fully digitized workflow, eScreening helps ensure the integrity and quality of clinical trial enrollment.

Accurate Trial Participant Identity Verification

  • Supports multiple verification methods to ensure authentic participant identity, including facial recognition, ID verification, fingerprint scanning, and signature capture
  • Implements closed-loop trial management with identity checks performed at each key stage, including check-in, check-out, duplication checks, and accommodation tracking
  • Automatically calculates washout periods to ensure there are no gaps or overlaps between trial participations

Data-Driven Participant Database Management

  • Manages detailed trial participant data with real-time enrollment risk alerts and a comprehensive overview of project status
  • Utilizes blacklists and whitelists to improve patient compliance and reduce enrollment risk
  • Provides high-coverage database support, enabling national and regional networking to enhance site capacity and strengthen trial participant risk management

Compliant, Efficient, and Fully Digitized Operations

  • Device registration and record-keeping utilize an identity verification interface to ensure legality and regulatory compliance
  • Fully digitized management and operations eliminate the need for manual data entry, reducing errors and improving efficiency

eScreening integrates within the broader Taimei Technology clinical trial ecosystem, complementing related products such as eCollect (EDC), eSitePro, and eTrialPro. The platform is designed to support compliant, streamlined participant management across clinical research sites at both regional and national levels.

Meta

Domain
Clinical Trial Management
Subdomain
Site Operations & Regulatory Documents
Software type(s)
Workflow Automation
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotechCRO
Development stage(s)
Clinical
Target user(s)
Lab Manager / Core Facility ManagerQA / Regulatory AffairsClinical / Diagnostic Professional
Compliance standard(s)
GxP