neuordo gives QA and regulatory teams an AI-powered assistant that tracks every document, flags every gap, and generates defensible compliance answers — so nothing slips through.
90%
fewer manually missed compliance gaps
1 click
audit-ready report generation
100%
answer source traceability
What your team deals with every week — and what neuordo eliminates.
Reconciling REACH, FDA 21 CFR, EU Cosmetics, and ISO requirements by hand is error-prone and time-consuming. Gaps get missed until they become audit findings.
COAs, SDSs, and spec sheets updated by suppliers without notice. Your team is never sure whether the version on file is the one that was submitted to the customer.
QA depends on R&D for formulation data, regulatory for approvals, and sales for context. Every questionnaire triggers a chain of interruptions across departments.
Compliance claims that are technically accurate but poorly worded can still trigger customer rejections or regulatory scrutiny. Precision matters in every statement.
Built for the precision and accountability that QA and regulatory work demands.
neuordo cross-references your product data against REACH, FDA, EU Cosmetics, California Prop 65, and other frameworks simultaneously — surfacing gaps before your customer does.
All COAs, SDSs, specifications, and certificates are indexed and versioned. neuordo alerts you when a document is expiring or a new supplier version is detected.
AI-generated answers are calibrated to regulatory standards — accurate, defensible, and consistent across every questionnaire your team submits.
Every generated answer, approval, and submission is logged with timestamp and user attribution. Audit-ready reports in one click.
Book a 30-minute demo and bring your own documents. We'll show you exactly what neuordo flags and generates.
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