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SYNeRA CTMS

Integrated clinical trial management with regulatory, site, safety, monitoring, and data capture modules in one system.

Solution by Symyoo
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Overview

SYNeRA™ CTMS is a Clinical Trial Management System developed by Symyoo STRC, designed to consolidate the full range of clinical trial operations into a single integrated platform. It is intended for organizations conducting clinical research who need to manage regulatory, operational, safety, and data functions within one system.

The platform is built to automate a large portion of routine tasks during clinical development, allowing teams to focus on critical decision-making. Its three-tier architectural design supports fast system implementation and easier system changes, while maintaining control over clinical operations. Integration with external data sources is supported through customized ETL processes or API connections.

CTMS Modules

  • Regulatory Management
  • Project Management
  • Site Management
  • Medical Safety Management
  • Risk-Based and Remote Monitoring
  • Site Monitoring
  • IRB/IEC Management
  • Network Management
  • Financial Management
  • Imaging Repository
  • Post-Market Safety Surveillance
  • Trial Master File

Electronic Data Capture (EDC) Modules

  • eCRF Collection
  • Study Design and Progress tracking
  • Scheduling and Reporting
  • Data Management
  • Subject Management
  • Medical Coding

Interactive Web Response System (IWRS)

  • IMP Supply Management
  • Randomization
  • Subject Enrollment

Integrated Services and Capabilities

  • Completely integrated information system for clinical trial and research management
  • EDC and Data Management modules function as the default core setup
  • Integrated IWRS supporting randomization methodologies ranging from simple permuted block randomization to covariate adaptive randomization
  • Integrated Investigational Product (IP) Accountability and Study Material Supply Management
  • Additional integrated modules including Project, Site, and User Management; Subject Management; Site Data Oversight through Central and Risk-Based Monitoring; Medical Safety Monitoring; Central Adjudication; Medical Coding; Trial Document Management; Financial Management; Clinical Network Management; and Dashboard functionality

SYNeRA™ CTMS is positioned as a full-package clinical research system with all individual modules operating under one platform. External data integration is available on request via customized ETL processes or API connections, supporting compatibility with existing clinical ecosystems.

Meta

Domain
Clinical Trial Management
Subdomain
Clinical Trial Management Systems (CTMS) & eTMF
Software type(s)
Workflow Automation
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotechCRO
Development stage(s)
ClinicalPost-Market & RWE
Target user(s)
QA / Regulatory AffairsClinical / Diagnostic ProfessionalIT / Systems Admin / Data Engineer
Compliance standard(s)
21 CFR Part 11GxP