Service
From data design to sharing and utilization,
complete it all with DataFlowService.
So you can focus solely on research, we make monitoring and tedious management tasks easier.
We provide AI-powered setup, research data validation, and tools for utilization and sharing — all in one platform.
AI-Powered Design
AI analyzes your protocol to help auto-generate eCRFs. Complex forms designed in minutes.
Automated Validation
Catch errors at the point of entry with real-time validation and auto-calculation logic.
Complete Audit Trail
Every change is automatically recorded to ensure data integrity.
Multi-site Collaboration
Conduct research across sites worldwide with real-time collaboration.
Every Step of Data Collection in One Platform
From study design to data collection, manage everything with an intuitive workflow.
Key Features
Everything you need for clinical research, all in one platform.
Study Design & Data Collection
AI-Powered Form Setup
AI analyzes protocol documents to auto-generate eCRFs. Even complex forms are designed in minutes.
Drag & Drop Form Builder
Build forms intuitively with a Collection → Form → Section → Item hierarchy — no coding required.
Protocol Versioning
Manage protocol amendments with version control while preserving previous version data.
Repeating Forms
Support for scheduled/unscheduled repeating collections and section repeats (fixed, sequential, enumerated).
Data Quality & Validation
Real-time Validation
Automatically check conditions at the point of data entry to catch errors instantly.
Auto-Calculation Logic
BMI, score totals, and more computed automatically via DataRule Methods — no manual errors.
Query Management
When data discrepancies are found, resolve them quickly with a query/response workflow.
Electronic Signatures
E-signatures for data approval, locking, and audit tracking.
Multi-site Research & Collaboration
Multi-site Support
Manage by organization type — Sponsor, Site, CRO, Lab — with per-site member assignment.
Randomization
Block randomization, stratification factors, and per-site allocation ratios.
Subject Matrix
View the entire data collection status at a glance with the Schedule of Events view.
Monitoring Support
Real-time data status dashboard with per-site progress tracking.
Data Integration & Analysis
Import / Export
Export/import project settings as ZIP with 3-step validation and atomic application.
ePRO Support
Patient Reported Outcome workflows where patients enter data directly.
CDISC Standards
CDASH/SDTM format data extraction.
API Integration
RESTful API for seamless data integration with external systems.
Support & Convenience
Inquiry System
Ticket system for inquiries, bug reports, and work requests with file attachments and comments.
Coordinator Service
Expert project setup assistance (4 hours/month included with Pro plan).
Multi-language
Korean / English / Japanese / Chinese — ready for international multi-site studies.
14-Day Free Trial
Try all features free for 2 weeks — no commitment required.
Security & Regulatory Readiness
Enterprise-grade security architecture to protect sensitive research data
Security Architecture
ICH-GCP Ready
Designed to meet international clinical trial standards
Electronic Records
Designed for electronic records & signatures regulations
AES-256 Encryption
KMS-based data encryption at rest
Complete Audit Trail
Full change history recorded & preserved
Ideal for These Studies
Flexible configurations tailored to various research types.
Investigator-Initiated Trials
- Rapid eCRF design with AI
- Cost-effective plans
- Expert setup support
Small-scale Clinical Trials
- Multi-site collaboration
- International clinical trial standards readiness
- Real-time monitoring support
Academic Research / Registry
- Flexible form design
- Long-term follow-up
- Data export capabilities
Get Started Today
Experience all features with a 14-day free trial