Go from protocol to live study in one afternoon.

Capture replaces your EDC, eConsent, ePRO, and randomization tools with one platform that costs less than your current audit trail software.

21 CFR Part 11 · HIPAA · No credit card required

10 min
Average time to first study
Free
Sandbox access
0
Sales calls required

Powering early-stage research at biotech sponsors · academic medical centers · CROs

21 CFR Part 11HIPAAGDPRGCP

You're running a 40-patient Phase II, not managing an aircraft carrier.

The Old Way

With Capture

6-month vendor procurement
Live in 10 minutes
$50k-$500k setup fees
Transparent, self-serve setup
Locked into 3-year contracts
Cancel anytime
Sales calls before you can try
Free sandbox, no demo required

How It Works

Three steps. One afternoon.

Step 1

Upload Your Protocol

Our AI reads your protocol and builds your study: forms, visits, randomization. Review and go live.

Step 2

Enroll Participants

Site-specific QR codes and links. eConsent built in. No app downloads for participants.

Step 3

Monitor Everything

Real-time dashboards, automated reminders, CDISC-ready exports. SDV and query management included.

Platform

One platform. Every tool you actually need.

Purpose-built for Phase I-III trials. No modules to buy. No features behind a paywall.

AI Study Builder

Upload your protocol PDF. Get a complete study in minutes.

ePRO & eCOA

15+ question types, branching logic, automated scoring.

eConsent

Digital signatures, version control, complete audit trail.

Casebook & CRF

Electronic case report forms with visit-level data capture.

Randomization

Stratified, block, and treatment arm assignment.

Visit Scheduling

Flexible windows, automated task generation per visit.

Multi-Site Management

Role-based access, per-site enrollment targets.

SDV & Monitoring

Source data verification and query workflows.

Safety & AE Reporting

Adverse event capture, grading, and tracking.

Real-time Analytics

Compliance dashboards and trend analysis.

Data Export

CSV, Excel, and XPT for CDISC submissions.

Action Items & Queries

Task management and issue resolution workflows.

Built for regulated research from day one.

Not bolted on after. Data residency in EU (Frankfurt) and USA (N. Virginia).

21 CFR Part 11HIPAAGDPR

FAQ

Questions we hear a lot.

Can I import my existing protocol?
Yes. Upload your protocol PDF and our AI Study Builder will generate your study structure (forms, visits, randomization) automatically. You review, tweak, and go live.
Do you support randomization?
Yes. Stratified block randomization with configurable treatment arms, allocation ratios, and stratification factors. Blinded and open-label designs supported.
What about source data verification?
Built-in SDV workflows. CRAs can verify CRF entries against source, raise queries, and track resolution. All within the platform with a complete audit trail.
Is this validated for regulatory submissions?
Capture is designed for 21 CFR Part 11 compliance with electronic signatures, audit trails, and role-based access controls. We provide a validation package for Enterprise customers.
How does the sandbox work?
The sandbox is a fully functional instance with all features enabled. Build your entire study, test workflows, and train your team. All free, no time limit, no credit card.
Can I export data for CDISC submissions?
Yes. Export in CSV, Excel, or XPT format. Data structures are designed with CDISC CDASH and SDTM mapping in mind.
Do participants need to download an app?
No. Participants access questionnaires and consent forms via mobile-friendly web links. Works on any device with a browser.
How is my data secured?
Encryption at rest and in transit, enterprise-grade security controls, HIPAA-compliant infrastructure, and data residency options in the EU (Frankfurt) and USA (N. Virginia).

Your next trial starts here.

Free sandbox. No sales call. No credit card.