Launching today

elsai Clinical Protocol Audit Agent

Launching today

AI-powered protocol governance and alignment for IRB review

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AI-powered protocol governance and alignment for IRB review

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elsai Clinical Protocol Audit Agent helps clinical and regulatory teams validate alignment across protocols, consent forms, and recruitment materials with governance before IRB submission. It provides AI-powered cross-document validation, amendment and version tracking, automated discrepancy detection, governance and audit traceability, IRB-ready review summaries, and integrates with CTMS, eIRB, eTMF, Word, and Google Docs workflows.

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Launch tags:Productivity•Artificial Intelligence•Tech

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Your own AI agent — 7 days free, then from $25/mo

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Clinical protocol reviews are still heavily dependent on manual line-by-line comparisons across protocols, consent forms, recruitment materials, and amendment versions. Small inconsistencies in eligibility criteria, risks, timelines, or participant compensation can lead to IRB delays, rework cycles, compliance risks, and audit challenges. Today, we’re launching the elsai Clinical Protocol Audit Agent — an AI-powered workflow assistant designed to help clinical and regulatory teams validate document alignment before submission. Key capabilities include: ✔ AI-powered cross-document validation ✔ Amendment and version tracking ✔ Automated discrepancy detection ✔ Governance and audit traceability ✔ IRB-ready review summaries ✔ Integration with CTMS, eIRB, eTMF, Word, and Google Docs workflows The goal is not to replace reviewers, but to help experts focus on critical clinical and regulatory decisions while reducing repetitive document review work. We’d love feedback from clinical operations, regulatory affairs, IRB teams, and research organizations.

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1d ago