Clinical Trial Software with Instant Study Setup

Clinical trial software with instant study setup: rapid build and deployment with eConsent, ePRO, and 21 CFR Part 11–aligned controls.

21 CFR Part 11–aligned · HIPAA-aligned security · No credit card required

Overview

Clinical Trial Software with Instant Study Setup

Clinical trial software with instant or rapid study setup lets you build and deploy studies quickly—without months of implementation. Teams want it to reach first patient or first dose as fast as possible. Capture provides EDC, eConsent, ePRO, and study builder in one platform; you can build and deploy in weeks, and for regulated studies we provide documentation to support validation and UAT. We avoid overclaiming “instant” for regulated studies; onboarding may include validation and sponsor-led UAT prior to go-live.

Why teams want instant or rapid study setup

Traditional EDC often requires long implementation. Rapid or streamlined study setup means you can configure visits, forms, and logic and go live quickly—with full audit trail and 21 CFR Part 11–aligned controls. For regulated studies, “instant” may not apply; we focus on rapid build and documentation to support your validation and UAT so you can go live as fast as your process allows.

Operational benefits of rapid study setup

Build and deploy studies in weeks; study builder to configure visits, forms, and logic
Full audit trail for all changes; 21 CFR Part 11–aligned controls and HIPAA-aligned security
One platform for EDC, eConsent, ePRO, and safety
For regulated studies: documentation to support validation and UAT (Enterprise)
Export for analysis and regulatory use

What slows teams down without rapid setup

Months of implementation before go-live
Heavy change control for simple updates
Delays to first patient or first dose
Need for speed without sacrificing compliance

Capture workflow for rapid study setup

Study builder and rapid deployment; all changes in audit trail
One platform for EDC, eConsent, ePRO, and safety; 21 CFR Part 11–aligned controls and HIPAA-aligned security
Build and deploy in weeks; for regulated studies, documentation for validation and UAT (Enterprise)
Export for analysis and regulatory use

Rapid study setup EDC EDC with automated study setup Features

FAQ

Questions we hear a lot

How fast can we set up a study in Capture?

Study build can start once you have protocol and CRF requirements. Many teams build and deploy in weeks. For regulated studies, we provide documentation to support validation and UAT (Enterprise); go-live depends on your validation process.

Is setup really instant for regulated studies?

For regulated studies, onboarding may include validation, documentation, and sponsor-led UAT prior to go-live. We provide the documentation you need to run that process efficiently; we don’t overclaim “instant” for regulated use.

Is Capture 21 CFR Part 11–aligned?

Yes. Capture is designed with 21 CFR Part 11–aligned controls and HIPAA-aligned security. We provide documentation to support sponsor validation when required (Enterprise).

Ready to see Capture in action?

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