Build questionnaires, collect ePRO data, and see results live - starting at $19 per participant. No sales calls. No contracts. No setup fees.
No credit card required • Cancel anytime • Export your data
Traditional platforms force you into 6-month procurement cycles, 6-figure setup fees, and pricing hidden behind NDA walls. You can't even try them without talking to sales.
We built the platform we wanted: transparent pricing, instant access, and clinical-grade tools that just work.
From questionnaire to live data collection - faster than filling out a grant application
Drag-and-drop editor with scales, multiple choice, open text, and skip logic. Use our templates or import your validated instruments.
Each site gets a unique link. Participants scan, consent, and start responding - no app downloads, no account creation.
Real-time dashboard shows enrollment, completion rates, and outlier detection. Export CDISC-compliant data anytime.
No hidden fees. No setup charges. Self-serve or enterprise - your choice.
Test the full platform with unlimited participants before going live
For pharma, CROs, and organizations requiring compliance packages
Typically responds within 24 hours
Enterprise alternatives: $50k-$500k+ setup fees
Test the full platform with unlimited participants before going live
Whether you're publishing research or running trials, we've got you covered
No procurement headaches. No enterprise sales cycles. Launch your study today.
Transparent costs that fit academic budgets. No hidden fees or surprise invoices.
Built-in consent forms and audit trails. Export everything your ethics board needs.
Launch pilot studies in hours, not months. No IT department required.
CDISC-compliant data exports with codebooks. Import directly into SPSS, R, or Python.
Collaborate with sites across institutions. Each site gets their own QR code.
Export anytime. No vendor lock-in. Your research, your control.
Patient-reported and clinician outcomes with real-time data capture. Schedule questionnaires, set reminders, track completion.
WYSIWYG consent builder with electronic signatures, versioning, and full audit trails. IRB-ready documentation.
Assign site coordinators, track enrollment by location, generate site-specific reports. Role-based permissions built-in.
Electronic data capture with CDISC-compliant exports. Data dictionaries, codebooks, and audit logs included.
Built for regulatory requirements. Versioning, audit trails, data integrity checks, and path to 21 CFR Part 11.
Live enrollment tracking, completion rates, outlier detection, and descriptive statistics. Monitor study health in real-time.
Your data stays yours. Encrypted, backed up, and exportable anytime. We're pursuing the certifications that matter.
Privacy-first architecture
Encryption at rest & in transit
Compliance roadmap in progress
Certification in progress
All data encrypted in transit and at rest. Role-based access controls. Complete audit trails. Regular security audits. SOC 2 Type II certification in progress.
Everything you need to know about launching studies on Capture.Study
Join researchers at top universities and biotech companies using Capture.Study to collect clinical data faster.
Questions? Email us at hello@capture.study