Clinical trial software for research institutes: EDC, eConsent, ePRO with 21 CFR Part 11–aligned controls. Lean teams, budget sensitivity.
21 CFR Part 11–aligned · HIPAA-aligned security · No credit card required
Overview
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–aligned 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).
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–aligned controls—without enterprise pricing or long implementation.
FAQ
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