Self-Serve Clinical Trial Software

Self-serve clinical trial software: build and run studies with eConsent, ePRO, and 21 CFR Part 11–aligned controls without long implementation.

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

Overview

Self-Serve Clinical Trial Software

Self-serve clinical trial software lets teams build and run studies without lengthy vendor-led implementation—study builder, eConsent, ePRO, and EDC in one platform so you can configure and amend studies when your process allows. Teams want it to move faster and keep control in-house. Capture provides EDC, eConsent, ePRO, and study builder in one platform with 21 CFR Part 11–aligned controls and HIPAA-aligned security; we provide documentation to support sponsor validation when required for regulated studies.

Why teams want self-serve clinical trial software

Vendor-led build often means long timelines. Self-serve means you can configure visits, forms, and logic—with full audit trail—and launch and amend studies without long vendor cycles. Operational benefits include rapid setup, flexible amendments, and one platform for consent, CRFs, and ePRO. For regulated studies, follow your validation and change-control procedures.

Operational benefits of self-serve software

  • Build and amend studies without long vendor-led implementation
  • Study builder to configure visits, forms, and logic; full audit trail
  • Same 21 CFR Part 11–aligned controls and HIPAA-aligned security for all data
  • One platform for EDC, eConsent, ePRO, and safety
  • Documentation to support sponsor validation when required (Enterprise)

What slows teams down without self-serve

  • Long vendor-led build and change control for simple updates
  • Dependency on vendor for form and visit changes
  • Delays to first patient or first dose
  • Need for rapid build and amendments without enterprise overhead

Capture workflow for self-serve clinical trial software

  • Study builder to configure visits, forms, and logic; all changes in audit trail
  • One platform for EDC, eConsent, ePRO, and safety; 21 CFR Part 11–aligned controls and HIPAA-aligned security
  • Rapid build and flexible amendments; documentation for validation (Enterprise)
  • Export for analysis and regulatory use

Related

Self-serve EDC platformsEDC with study builderFeatures

FAQ

Questions we hear a lot

What is self-serve clinical trial software?
Self-serve means you can build and amend studies using the study builder without lengthy vendor-led implementation. Capture includes study builder so you can configure visits, forms, and logic; all changes are tracked in the audit trail.
Is Capture self-serve?
Yes. Capture includes a study builder so you can build and amend studies. We provide documentation and support for qualification and UAT when required for regulated studies (Enterprise).
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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