Clinical Trial Software for Research Institutes

Clinical trial software for research institutes: EDC, eConsent, ePRO with 21 CFR Part 11–compliant controls. Lean teams, budget sensitivity.

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

  • ISO 27001 certified
  • 21 CFR Part 11 compliant
  • GDPR compliant
  • EU and US data hosting
  • HIPAA compliant
  • ICH GCP E6(R3) compliant
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Overview

Clinical Trial Software for Research Institutes

Clinical trial software for research institutes supports investigator-led and academic research with one platform for EDC, eConsent, and ePRO—with 21 CFR Part 11–compliant controls and fit for lean teams and smaller budgets. Why academic studies differ: often investigator-led, budget-sensitive, and lean staffing. Budget and staffing realities mean research institutes need one system without enterprise pricing. Capture fit: one platform for EDC, eConsent, ePRO; pricing and support that fit academic use; documentation for sponsor validation when required (Enterprise).

Why academic studies differ

Research institute trials are often investigator-led, with lean teams and budget sensitivity. Teams need one platform for consent and data capture—with full audit trail and 21 CFR Part 11–compliant controls—without enterprise pricing or long implementation.

Budget and staffing realities

  • One platform for EDC, eConsent, ePRO; one audit trail
  • Pricing and support that fit institute budgets and lean teams
  • Same 21 CFR Part 11–compliant controls and HIPAA-compliant security
  • Study builder for investigator-led build and amendments
  • Documentation to support sponsor validation when required (Enterprise)

Key pain points

  • Enterprise software pricing that doesn’t fit institute budgets
  • Long implementation for lean teams
  • Need for one platform for consent, CRFs, and ePRO with one audit trail
  • Capture: fit for research institute use

Capture fit for research institutes

  • One platform for EDC, eConsent, ePRO; fit for academic and research institute use
  • 21 CFR Part 11–compliant controls and HIPAA-compliant security
  • Pricing and support that fit lean teams and institute budgets
  • Explore use case or book a demo
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Related

Clinical trial software for universitiesSoftware for investigator-initiated trialsFeatures

FAQ

Questions we hear a lot

What is clinical trial software for research institutes?
Clinical trial software for research institutes supports investigator-led research with one platform for EDC, eConsent, and ePRO—with 21 CFR Part 11–compliant controls and fit for lean teams and institute budgets.
Is Capture 21 CFR Part 11–compliant?
Yes. Capture is designed with 21 CFR Part 11–compliant controls and HIPAA-compliant security. We provide documentation to support sponsor validation when required (Enterprise).

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