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 ![Litewave AI](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_e8b08f420095f55b53228f6ebe72161c/litewave-ai.jpeg "Litewave AI")
](/products/litewave-ai/reviews)

# Litewave AI Discussions

Litewave AI is an AI quality review platform for regulated manufacturers, including pharma CDMOs, medical device, dietary supplement, food and cosmetics companies. It automates review of batch records, device history records (DHRs), certificates of analysis (CoAs) and supplier documents by checking them against specs, approved supplier lists and required tests, then flags discrepancies with every finding linked to its source page and field. Quality teams review exceptions and sign off, keeping records audit-ready for FDA, NSF, SQF and customer audits. Litewave works with paper and handwritten records or digitized workflows, and runs on top of existing MES, QMS, LIMS and ERP systems, so nothing needs to be replaced. The same structured data feeds quality and manufacturing analytics, surfacing trends across batches, sites and suppliers. Deployment options include on-premises or within the customer’s own cloud environment. Common use cases: batch record and DHR review, supplier CoA verification, paper-to-digital batch records, audit readiness and quality analytics.

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