Investigator Portal for Clinical Trials

Investigator portal for clinical trials: one place for enrollment, consent, and data capture. 21 CFR Part 11–aligned controls.

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

Overview

Investigator Portal for Clinical Trials

An investigator portal for clinical trials gives investigators and site staff 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).

Who this role is and daily workflow

An investigator portal should provide 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, the portal is one place for study tasks; when they’re separate, administrative burden increases.

Daily workflow

  • Screening and enrollment in same platform as consent and CRFs
  • eConsent and EDC in one place; one audit trail
  • Same 21 CFR Part 11–aligned controls and HIPAA-aligned security
  • ePRO and visit-based data capture in same platform
  • Documentation to support sponsor validation when required (Enterprise)

Key pain points

  • Multiple systems for screening, consent, and data capture
  • Paper consent and manual handoffs
  • Fragmented data and duplicate entry
  • Need for one portal that reduces administrative burden

Capture fit for investigator portal

  • One platform for EDC, eConsent, ePRO, and enrollment; one audit trail
  • 21 CFR Part 11–aligned controls and HIPAA-aligned security
  • Investigators and site staff use one system for study tasks
  • See how sites use it or book a demo

Related

Clinical trial software for investigatorsSoftware for research coordinatorsFeatures

FAQ

Questions we hear a lot

What is an investigator portal for clinical trials?
An investigator portal gives investigators and site staff one place for screening, consent, and data capture—with 21 CFR Part 11–aligned controls. Capture includes EDC, eConsent, ePRO, and enrollment in one platform.
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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