Affordable EDC for Clinical Trials

Affordable EDC for clinical trials: eConsent, ePRO, and 21 CFR Part 11–aligned controls without enterprise pricing. See how it works.

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

Overview

Affordable EDC for Clinical Trials

Teams running early-phase or small studies often need affordable EDC that still delivers 21 CFR Part 11–aligned controls, integrated eConsent and ePRO, and one audit trail—without enterprise pricing or long implementation. Cost and complexity can block study start or force compromises on compliance. Modern tools change that: one platform for EDC, eConsent, and ePRO with pricing that scales with study size and rapid build so you can launch without big upfront spend. Capture fits teams that want compliant, integrated EDC without enterprise overhead.

What slows teams down without affordable EDC

Enterprise EDC often comes with high per-seat or per-study minimums, long implementation, and heavy change control. Small teams and early-phase sponsors get stuck: either pay for capacity they don’t need or patch together spreadsheets and paper. Affordable EDC means pricing that fits your cohort size, rapid setup, and one platform for consent and data capture—with full audit trail and 21 CFR Part 11–aligned controls so you don’t sacrifice compliance for cost.

What modern tools change

  • Pricing that scales with study or cohort size instead of enterprise minimums
  • One platform for EDC, eConsent, and ePRO; one audit trail
  • Rapid study build and deployment without months of vendor-led implementation
  • 21 CFR Part 11–aligned controls and HIPAA-aligned security
  • Documentation to support sponsor validation when required (Enterprise)
  • Export for analysis and regulatory use

Pain points without affordable EDC

  • Enterprise pricing that doesn’t fit early-phase or small-study budgets
  • Per-seat or per-module minimums that burn budget before first patient
  • Long implementation cycles that delay study start
  • Need for compliant EDC without enterprise cost or complexity

Capture fit

  • Single platform for EDC, eConsent, ePRO, and safety; pricing that scales with study size
  • 21 CFR Part 11–aligned controls and HIPAA-aligned security
  • Rapid build and amendments; documentation for sponsor validation (Enterprise)
  • See how it works or book a demo to evaluate fit

Related

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FAQ

Questions we hear a lot

What makes EDC affordable for clinical trials?
Affordable EDC typically means pricing that scales with study or cohort size, rapid setup, and one platform for consent and data capture—with 21 CFR Part 11–aligned controls. Capture offers plans that scale; see pricing and book a demo to evaluate fit.
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).
Can we use Capture for small studies?
Yes. Capture is built for early-phase and small-to-mid-size trials. You get one platform with eConsent, ePRO, and EDC; pricing scales with study size.

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