Clinical trial software for investigators: reduce administrative burden and keep study tasks in one place. 21 CFR Part 11–aligned controls.
21 CFR Part 11–aligned · HIPAA-aligned security · No credit card required
Overview
Clinical trial software for investigators supports sites and coordinators with one place for enrollment, consent, and data capture—reducing administrative burden and keeping study tasks in one system with 21 CFR Part 11–aligned controls. Who this role is: investigators and site staff run studies day to day. Daily workflow includes screening, consent, CRF entry, and ePRO. Key pain points: multiple systems, paper consent, and fragmented data. Capture fit: one platform for EDC, eConsent, ePRO, and enrollment; one audit trail; documentation for sponsor validation (Enterprise).
Investigators and site staff need one system for screening, consent, and data capture—with full audit trail and 21 CFR Part 11–aligned controls. When enrollment, eConsent, and EDC are in one platform, sites have one place for study tasks; when they’re separate, administrative burden and fragmentation increase.
FAQ
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