ENVERALIGN
Microsoft Word Native • 21 CFR Part 11 Aligned

AI Embedded for Speed.
Grounded in Clinical Truth.

The zero-hallucination agentic writing suite embedded natively inside desktop Microsoft Word. Linking draft narrative claims directly to immutable Clinical Study Report (CSR) coordinates and federated registries.

Clinical Application Layer

Active Clinical Workflows

Purpose-built modules integrated natively into desktop Microsoft Word for Medical Affairs and Regulatory teams.

✍️ Enveralign Drafter

Available in Pilot

Accelerates CSR-to-manuscript transformations, section summaries, and structured outlines while preserving rigorous medical narrative coherence.

Senior Medical Writers Powered by Enveralign AI™

🛡️ Enveralign Audit

Available in Pilot

Deterministic reference checking, live registry concordance auditing, and ICMJE author compliance verification inside active Word documents.

QC Editors & Authors Powered by Enveralign AI™

Looking for Protocol-to-CSR validation or congress intelligence? Inquire about our upcoming co-development tracks.

Underlying Core Engine

Enveralign AI™ Engine Infrastructure

Deterministic coordinate extraction engines and cryptographic audit pipelines powering every application.

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MS Word Co-Location

Zero context switching. Authors draft, redline, and inspect sources directly within desktop Word through an integrated sidebar interface.

M365 Enterprise Ready
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[p. X, Line Y] Provenance

100% deterministic coordinate anchors. Every extracted statistic binds to exact CSR PDF line items and tables.

Zero Hallucinations
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Federated Audit

Asynchronous live PubMed (PMID), CrossRef (DOI), and ClinicalTrials.gov (NCT) validation with deterministic metadata concordance.

NEJM • Lancet • JCO
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Enterprise Isolation

Dedicated virtual private cloud deployment, customer-managed encryption keys (CMEK), and automated zero-retention data pipelines.

Zero Data Retention (ZDR)
HITL

Human-in-the-Loop by Design • ICMJE Compliant

AI never publishes or commits unilaterally. Enveralign AI acts exclusively as an assistive agent—extracting, redlining, and auditing—while human medical authors retain 100% editorial authority, final sign-off, and accountability backed by an immutable 21 CFR Part 11 audit trail.

14-Day Design Partner Pilot Program

Deploy to 1–2 senior medical writing editors. Benchmark QC velocity across active clinical trial drafts against source CSRs.