Quality leaders in regulated healthcare and life sciences do life-critical work, and most are doing it with a quality system that makes it harder than it should be. Documents in SharePoint. CAPAs in Excel. Training records in email. Equipment logs on a wall calendar. Every audit cycle turns into a fire drill.
Kintavo replaces all of it.

Kintavo is the AI-native eQMS that unifies every quality and compliance function into one configurable platform — where every record, workflow, and compliance event is linked to everything else. Document control, training, CAPA, deviations, audits, change control, risk, and supplier quality. Equipment, calibration, preventive maintenance, and QC analysis. Plus an intelligence layer — AI Smart Assist™, Audit Intelligence™, and the 360° Compliance Map™ — that surfaces gaps before an inspector ever finds them.

What makes us different:
Configuration belongs to your quality team. Build and change workflows yourself with a visual builder — no IT tickets, no vendor change requests. When regulations change, you adapt the same day.

Compliance is built in, not bolted on. 21 CFR Part 11, ISO 13485, GxP, AABB, CAP, CLIA, SOC 2, and HIPAA — with IQ/OQ/PQ validation documentation included in every implementation.

Purpose-built for the work. From blood banks and clinical labs to pharma, biotech, and cell & gene therapy — including the only mid-market eQMS with a dedicated Cell Therapy operations module.

The result: audits become predictable instead of frantic, compliance becomes a baseline instead of a burden, and your team gets time back for what actually matters — innovation and patient safety.

Before: overwhelmed. After: empowered.

📧 Email us at info@kintavo.com

🌐 Learn more at kintavo.com

Kintavo eQMS and Workflow Platform

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Kintavo eQMS and Workflow Platform

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