SYNeRA™ CTMS:
All-in-one clinical trial platform

Symyoo STRC has developed SYNeRA™ Clinical Trial Management System (CTMS), which has tens of system modules completely integrated in ONE roof.

SYNeRA™ CTMS automates the majority of routine clinical trial activities through a fully integrated digital platform, enabling study teams to spend less time on manual processes and more time making informed decisions that drive study success.

By bringing EDC, RTSM, Medical Safety, Monitoring, Trial Management, and other essential functions together in one unified platform, SYNeRA™ CTMS eliminates fragmented workflows, reduces operational complexity, and ensures a single source of truth across the entire clinical trial lifecycle.

With real-time data visibility, intelligent workflow automation, and seamless integration with external clinical systems, SYNeRA™ CTMS helps sponsors, CROs, and research sites accelerate study startup, improve operational efficiency, enhance data quality, and maintain regulatory compliance.

SYNeRA™ CTMS is more than a CTMS—it’s a complete clinical research platform that transforms the way modern clinical trials are managed.

 

Everything Your Clinical Trial Needs.
One Platform.

SYNeRA™ CTMS is a comprehensive clinical research platform that brings together every essential function required to plan, manage, monitor, and oversee clinical trials—all within a single integrated system.

Unlike conventional solutions that require multiple standalone applications, SYNeRA™ CTMS seamlessly integrates Electronic Data Capture (EDC), Randomization & Trial Supply Management (RTSM), Medical Safety, Risk-Based Monitoring, Site & Project Management, Trial Document Management, Subject Management, Data Management, Medical Coding, Reporting, and many more modules into one unified platform.

As the first affordable, full-package clinical research system, SYNeRA™ CTMS eliminates the complexity of managing multiple vendors, disconnected databases, and fragmented workflows. One platform means one login, one database, one source of truth, and one seamless user experience.

Built on a flexible three-tier architecture, the platform enables rapid implementation, simplified customization, and scalable performance while providing complete control over every aspect of clinical trial operations.

SYNeRA™ CTMS also integrates seamlessly with your existing clinical ecosystem. Through customized ETL (Extract, Transform, Load) processes or secure APIs (Application Programming Interfaces), data can be exchanged effortlessly with EMR, laboratory systems, ePRO, imaging platforms, and other external applications.

From study startup and patient enrollment to monitoring, medical safety oversight, and database lock, SYNeRA™ CTMS supports the entire clinical trial lifecycle in one intelligent platform.

 

One Intelligent Platform, New Insight: Beyond CTMS
SYNeRATM CTMS
Capabilities

SYNeRA™ CTMS is a comprehensive, end-to-end platform that integrates every essential function required to manage modern clinical trials—from study startup to database lock and medical safety oversight.

    • Clinical Trial Operations
      • Study & Project Management
      • Site Management
      • Subject Management
      • User & Role Management
      • Visit & Schedule Management
    • Clinical Data Management
      • Electronic Data Capture (EDC)
      • Data Validation & Query Management
      • Medical Coding (MedDRA/WHO Drug)
      • Reporting & Analytics
    • Randomization & Trial Supply
      • RTSM (Randomization & Trial Supply Management)
      • From Permuted Block Randomization to Covariate Adaptive Randomization
      • Investigational Product (IP) Accountability
      • Clinical Supply & Inventory Management
    • Clinical Monitoring
      • Risk-Based Monitoring (RBM)
      • Remote, Central Monitoring
      • Monitoring Visit Management
      • Monitoring Report and Issue Follow-up
    • Medical Safety
      • Medical Safety Oversight
      • SAE Case Management
      • Medical Review
      • Central Adjudication
    • Trial Documents & Compliance
      • Electronic Trial Document Management
      • Regulatory Document Management
      • Audit Trail
      • Regulatory Compliance: 21 CFR Part 11 Compliance
    • Integration & Intelligence
      • Real-Time Dashboards & Business Intelligence
      • Smart Alert System: To-Do List, Email and Event Management
      • API & ETL Integration: EMR/LIS/External System Connectivity
      • AI-Ready Clinical Data Platform