Capture.Study is EDC software for clinical trials. Build forms, capture data, and stay compliant with 21 CFR Part 11, GCP, GDPR, and HIPAA. Try it free, no credit card needed.
Electronic Data Capture (EDC) is the software clinical research teams use to collect, store, and manage trial data digitally instead of on paper. It replaces binders, fax machines, and spreadsheets with structured electronic forms that capture data at the point of care.
Good EDC software saves weeks of setup time, reduces transcription errors, and keeps your data audit-ready from Day 1. Capture.Study does all of that and lets you try it for free before you commit.
Most EDC platforms are built for 5,000-patient Phase III trials. Yours is probably smaller. You should not pay like it is not.
The Old Way
With Capture
Ready to stop overpaying for EDC?
How It Works
No procurement process. No vendor kickoff calls. No waiting.
Sign up free. Create your study, set your visit schedule, and build CRFs with the drag-and-drop form builder. Use a template or start from scratch.
Enter sample data, check your skip logic, review audit trails, and export test data. Fix everything before a single real patient is enrolled. All free.
Activate your study. Add sites, invite coordinators, and start enrolling. Your data is captured with a complete audit trail from the first entry.
Platform
One platform. No bolt-ons. Every module below is included in your subscription.
Upload your protocol PDF. AI reads it and generates your study structure, forms, and visit schedule. Review, adjust, go live.
15+ field types including scales, sliders, date pickers, and repeating groups. Add branching logic so each form only shows what matters.
Present consent documents on any device. Participants sign electronically with full audit trail and witness co-signatures.
Enroll participants, assign them to sites, and track status across every visit. Import from CSV or invite by email.
Define visit schedules with configurable windows. Each visit auto-generates the right tasks for coordinators.
Stratified block randomization with treatment arm assignment. Blinded and open-label designs with emergency unblinding.
Show or hide questions based on answers. Flag out-of-range values in real time. Reduce queries before they happen.
See enrollment, form completion, query counts, and compliance metrics live. No waiting for reports.
Export any time in CSV, Excel, or SAS XPT. CDISC-ready for regulatory submissions. No vendor lock-in.
CRAs review data remotely, raise queries, and track resolution. Built-in monitoring visit reports.
Add sites, assign staff roles, manage permissions. Each site sees only its own participants.
Capture adverse events with grading, causality, and outcome tracking. All linked to the participant record.
All features included. No modules to buy separately.
Compliance is not an add-on. It is built into every part of the platform. Data residency in EU (Frankfurt) and USA (N. Virginia).
Every data entry, edit, and signature is logged with a timestamp, user identity, and reason for change. Always available for export. No configuration needed.
Why Capture
Build your entire study, create all your forms, test with sample data, and export results. No time limit, no credit card. You only pay when you go live with real participants.
No servers to provision, no software to install, no vendor implementation project. Sign up, build your forms, and start collecting data.
eCRFs, eConsent, randomization, monitoring, ePRO, AE reporting, recruitment, and notifications. One platform, one login, one validation.
Export your data any time in CSV, Excel, or SAS XPT format. If you decide to leave, you take everything with you.
A 30-patient Phase II should not cost the same as a 5,000-patient Phase III. You pay per participant, so costs scale with your actual study.
Create your free account, build your forms, and test with sample data.
No credit card. No sales call. No commitment.