Everything you need for clinical trials and research studies. From electronic patient-reported outcomes to multi-site data management, all in one modern platform with transparent pricing.
Comprehensive platform covering every aspect of modern clinical research
Electronic Patient-Reported Outcomes and Clinical Outcome Assessments
Electronic Data Capture for clinical research
Electronic informed consent with digital signatures
Coordinate research across multiple locations
Insights and reporting for research teams
Enterprise-grade security and regulatory readiness
Electronic Patient-Reported Outcomes & Clinical Outcome Assessments
Responsive design works on any device
Scan to enroll, no app install required
10+ question formats including scales, sliders, text, multiple choice
Conditional questions based on responses
Responses instantly available to researchers
Pre-built templates for sleep, pain, symptoms
Support both anonymous research and identified clinical trials
Daily, weekly, or event-triggered questionnaires
Track changes and maintain data integrity
Deploy questionnaires in multiple languages
Collect data without internet, sync later
SMS and email reminders for compliance
Real-time electronic data capture and clinical data management
Live view of enrollment and responses
Track completion rates and participant engagement
Export raw and decoded data for analysis
Track all data changes with timestamps
Min/max limits, required fields, format checks
Mean, SD, median, IQR, outlier detection
Visual data distribution analysis
Analyze data by time windows
Close and archive studies when complete
Automatic codebook with exports
Raise and resolve data queries
SDV workflow for monitors
Standards-compliant data formats
Document why data was edited
Digital informed consent with signatures and audit trails
Create section-based consent forms
HTML5 canvas signature collection
Track consent form changes over time
IP address, timestamp, device info
Download signed documents
Trigger re-consent when forms change
Deploy in participant's language
Document when participants withdraw
Coordinate research across multiple clinical sites
QR codes unique to each site
Format: SITE-NUMBER (e.g., 001-0042)
Separate views for site staff
Site coordinators see names, researchers see coded IDs
Analyze data per site
Enrollment rates, completion rates by site
Export data for specific sites
Track protocol deviations by site
IRB approval tracking per site
Risk-based monitoring across sites
Real-time insights and statistical analysis
See participant counts live
Track questionnaire compliance
N, mean, SD, median, IQR, min, max
Z-score based outlier flagging
Box plots, distribution charts
Time-windowed data views
Compare metrics across sites
Last activity, response history
Build your own analysis views
Email reports weekly/monthly
Enterprise-grade security and regulatory readiness
Encrypted data storage and transmission
Privacy-first data architecture
Researcher, site coordinator, admin roles
Database-level data isolation
Comprehensive activity tracking
AES-256 encryption
Secure data transmission
Privacy-preserving research
Regulatory framework readiness
Third-party security audit
Track old/new values for every edit
Cryptographic proof of identity
Privacy-first architecture
Encryption at rest & in transit
Compliance roadmap in progress
Certification in progress
Flexible question formats for any clinical assessment or patient diary
Short or long text responses
Use case: Open-ended feedback, comments
Integer or decimal numbers
Use case: Age, weight, dosage, counts
Rating scales (1-5, 1-10, etc.)
Use case: Pain scores, satisfaction ratings
Visual slider with numeric output
Use case: Visual analog scales, intensity ratings
Select one option from a list
Use case: Yes/No, gender, single selection
Select multiple options
Use case: Symptoms checklist, medication list
Select from dropdown menu
Use case: Country, state, long option lists
Calendar date selection
Use case: Date of birth, event dates
Time of day selection
Use case: Medication timing, symptom onset
Multi-line text input
Use case: Detailed notes, adverse event descriptions
See how we compare to traditional enterprise EDC systems
| Feature | Capture.Study | Enterprise EDC |
|---|---|---|
| Free Sandbox Trial | ||
| Public Pricing | ||
| No Sales Call Required | ||
| Setup Time | < 1 hour | 2-4 weeks |
| Per-Participant Pricing | $19/month | Contact Sales |
| ePRO / eCOA | ||
| EDC | ||
| eConsent | ||
| Multi-Site Support | ||
| Real-Time Data | ||
| Mobile-Optimized | Varies | |
| Skip Logic / Branching | ||
| QR Code Enrollment | ||
| Template Library | ||
| HIPAA-Ready | ||
| 21 CFR Part 11 Path | Coming Soon |
Start fast with validated templates for common clinical assessments
Browse All TemplatesEverything you need to know about Capture.Study
Join the waitlist for early access to the only ePRO platform with public pricing and free sandbox trials.
Transparent pricing: $19 per participant per month