Discover Pricing
Talk to an expert
Highly rated by clinical research professionals | 
4.2 / 5 stars
Electronic Data Capture
Launch clinical data capture in days, not months.
Design eCRFs, collect study data, manage queries, and maintain data quality in a validated EDC environment built for clinical research.
Key benefits
- Platform live within 5 business days
- Flexible pricing that scales with your research
- ROI within 6 months according to G2 users
Trusted by clinical research professionals
Based on 400+ independent user reviews, ResearchManager EDC has been recognised as a High Performer and awarded Highest ROI on G2.
What sets ResearchManager EDC apart?
AI-powered study insights
- Ask questions in natural language
- Instant answers from live study data
- No reports or exports required
- Faster decision-making
Only invest when research grows
- Pay only for active studies
- Start with a single study with On Demand
- Move to the Enterprise plan as study portfolios grow
- No platform migration when scaling
Maintain full control over study configuration
- Build and manage eCRFs without coding
- Make changes without vendor dependency
- Full control over study workflows
- Designed for research teams, not developers
Start with EDC, expand when needed
- Standalone EDC or complete Clinical Research Suite
- Add ePRO, eConsent, RTSM, CTMS, and eTMF
- No platform migration as requirements grow
- One vendor across the research lifecycle
Built for compliant clinical research
Key Features
Study Design
- No-code eCRF design
- Protocol-driven study setup
- AI-powered Insights
- Reusable templates and form libraries
- Recurring questionnaires
- Single and multicenter studies
Data Collection & Quality
- Advanced validations
- Query management
- Real-time dashboards
- Audit trails
- Database lock
Security & Integrations
- REST API
- Single Sign-On (SSO)
- Role-based permissions
- Electronic signatures
- Two-factor authentication
First study configuration is on us
Getting started with a new EDC shouldn’t require months of setup.
Our GCP-trained consultants configure the first study and eCRFs according to the study protocol at no additional cost.
Included
- eCRF configuration
- Study setup
- Validation rules
- Workflow configuration
Trusted by over 200 organizations
For more than 13 years, CROs, sponsors, universities and healthcare organizations have relied on Clinical Research Suite every day for structured and reliable clinical research. Find out how we help organizations conduct studies more efficiently, compliantly and with complete control.
Hans Middelweerd
Global Sales Manager - Academic & Non-Profit
Thierry Wetting
Global Sales Manager - CROs & Sponsors
