Fastest Way to Launch a Clinical Trial

Fastest way to launch a clinical trial: EDC with eConsent, ePRO, and 21 CFR Part 11–aligned controls. Rapid build and deployment.

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

Overview

Fastest Way to Launch a Clinical Trial

The fastest way to launch a clinical trial is to use one platform for EDC, eConsent, and ePRO with rapid build and deployment—so you’re not waiting months for vendor-led implementation. What slows teams down is long setup cycles and heavy change control; what modern tools change is study builder and rapid go-live with 21 CFR Part 11–aligned controls. For regulated studies, onboarding may include validation and sponsor-led UAT; we provide documentation to support that process. Capture fits teams that want to reach first patient or first dose as fast as their process allows.

What slows teams down

Traditional EDC often requires months of implementation, complex change control for simple form updates, and dependency on vendor for build and amendments. The fastest path to launch is one platform with study builder, integrated eConsent and ePRO, and documentation to support validation—so you can build, qualify, and go live without lengthy vendor cycles.

What modern tools change

  • Study builder to configure visits, forms, and logic; rapid deployment
  • One platform for EDC, eConsent, ePRO, and safety; one audit trail
  • Amend without lengthy vendor cycles when your process allows
  • 21 CFR Part 11–aligned controls; documentation for validation (Enterprise)
  • For regulated studies: validation and UAT support so you can go live efficiently

Pain points

  • Months of implementation before go-live
  • Heavy change control for simple form and visit updates
  • Vendor dependency for build and amendments
  • Need for speed without sacrificing compliance

Capture fit

  • Study builder and rapid deployment; all changes in audit trail
  • One platform for EDC, eConsent, ePRO, and safety; 21 CFR Part 11–aligned controls
  • Documentation for sponsor validation (Enterprise); see how it works or book a demo

Related

Rapid study setup EDCEDC with study builderFeatures

FAQ

Questions we hear a lot

What is the fastest way to launch a clinical trial?
Use one platform for EDC, eConsent, and ePRO with rapid build and deployment. Capture includes a study builder so you can configure and go live quickly; for regulated studies we provide documentation to support validation and UAT.
Is setup really fast 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.
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).

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