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eSafety
Pharmacovigilance Compliance Management System

End-to-End Quality and Compliance in Drug Safety Monitoring

Comprehensive Pharmacovigilance

throughout the Entire Product Lifecycle

Pre-Market + Post-Market

Product Safety Data

GVP & Regulatory Compliance and Efficient Operations

Regulatory Compliance with Smart System Management

GVP-Based Unified Management
Unified management of institutions, personnel, policies, and resources based on GVP requirements

Digital System Visualization
Visualize system management and pharmacovigilance activities

Real-Time Data Synchronization
Generate and automatically update the main pharmacovigilance system files with one click

Automated Compliance Checks
Automatically detect compliance issues and provide intelligent corrective guidance

Intelligent Safety Data Processing that's Compliant, Efficient, & Cost-effective

  • Collect, process, and submit safety data from various sources with risk control and management

  • Unified management of adverse reaction reports with statistical analysis, signal alerts, and audit trails

  • Integration with CDE and CDR systems for direct adverse reaction reporting via E2B

  • Compliant with global pharmacovigilance databases, supporting direct submissions to FDA FAERS and EU EudraVigilance

Validated Literature Search

  • Supports searches across CNKI, Chinese Medical Journals, PubMed, and Elsevier in both English and Chinese

  • Ensures compliance with search sources

  • Customizable search queries and frequency settings

  • Compliant full-text downloads with search traceability

Risk Alerts and Management with AI-Assisted Decision Making

Signal Detection & Intelligent Alerts

Automatically collect AE data from FDA, WHO, EMA, and eSafety databases. Invalid reports are filtered out, with multi-dimensional views of product overviews, report distribution, signal lists, and trends

Adverse Reaction
Analytics

Over 35 statistical charts updated daily, providing in-depth analysis of individual case reports. Exportable in Excel, PDF, and other formats for ease of use

Compliance
Risk Alerts

Visualize risks and quickly identify pharmacovigilance compliance issues. Automatically generate risk lists, solutions, and risk review reports

Automated Pharmacovigilance : Replacing Manual Tasks to Improve Efficiency

  • Using humanoid robots for pharmacovigilance data processing, including MedDRA coding, document archiving, and individual case report tracking

  • Automating repetitive, mechanical, and rule-based tasks reduces labor costs and error rates while enhancing work efficiency

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