Trust Center
Trust posture, plainly stated.
OpenIRB exists to make review more accountable. That begins with our own claims.
Current capabilities
Category definition
Public category definition: reviewable intelligence.
Operating model
Draft operating model for Intelligent Review Boards.
Website & PRD
Website PRD and final copy for OpenIRB.org.
Standards companion
Companion institutional standards architecture through IRB.Institute.
Ecosystem model
Ecosystem mapping to EXOCHAIN, CyberMedica, and AI-SDLC Institute.
Artifact model
Conceptual artifact model: intake, evidence packet, classification, decision artifact, registry metadata, continuing review.
In formation
Public docs
Conceptual documentation and draft schemas.
Registry model
Public/permissioned registry design.
Early access pilots
Institutional pilots and implementation guide.
Reference workflows
Board templates and reference review workflows.
Open-source structure
Open-source repository structure and governance model.
Custody integration
Optional EXOCHAIN trust receipt integration.
Not yet claimed
OpenIRB does not currently claim:
- To be a legally registered Institutional Review Board.
- To replace required IRB review, FDA review, OHRP compliance, legal advice, medical judgment, or institutional policy.
- To certify AI safety, legality, ethics, clinical effectiveness, or regulatory compliance.
- To operate a production public registry of regulated or sensitive review records.
- To have completed independent security, SOC 2, ISO, or regulatory audits unless a linked artifact says otherwise.
Do not submit sensitive data. OpenIRB public forms and early access inquiries should not be used to submit protected health information, confidential participant data, regulated study materials, trade secrets, credentials, API keys, or model secrets. The site is static-first, privacy-preserving, and protected with modern security headers and a nonce-based Content-Security-Policy.