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SYNeRA EDC

Clinical data collection and management with real-time validity checks, data monitoring, and subject tracking for complex trials.

Solution by Symyoo
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Overview

SYNeRA™ EDC is an Electronic Data Capture system developed by SYMYOO for collecting and managing clinical study data across trials of varying complexity. It is designed to support both complexly designed late-phase trials and lower-budget Investigator Initiated Trials (IIT).

The system covers the full data management workflow — from data collection through data cleaning to data analysis — using tools such as instant data validity checks, skip logics, data clarification requests, and centralized data monitoring. Its design aims to reduce data collection errors and provide investigators and researchers with real-time access to study data.

E-Data Capture

  • Data collection with validity checks and rule-based validation
  • Data clarification request functionality
  • Centralized data monitoring
  • Various data management supporting tools

Study Design and Progress

  • Study visit sequence management
  • CRF data collection scheduling
  • Site enrollment summary
  • Study progress summary reporting

Subject Management

  • Subject screening and enrollment
  • Subject randomization supporting both permuted block and adaptive methods
  • Subject progress tracking and reporting
  • Investigational product accountability

Supporting Tools

  • AE/SAE reporting
  • Medical coding
  • Project, site, subject, and data management reports
  • DSMB and custom reports

Service Capabilities

  • Advanced information system for clinical research data collection and management
  • Fully data quality assured EDC as a core offering
  • Integration with IWRS (Interactive Web-based Randomization System) and Supply Chain Management systems

Meta

Domain
Clinical Trial Management
Subdomain
Electronic Data Capture (EDC)
Software type(s)
Record-Keeping System
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
Academic / ResearchBiotechCROPharma
Development stage(s)
ClinicalPost-Market & RWE
Target user(s)
Research ScientistQA / Regulatory AffairsClinical / Diagnostic Professional
Compliance standard(s)
21 CFR Part 11GxP