BatchLine
BatchLine Lite MES helps pharmaceutical and GxP-regulated companies digitize manufacturing, quality, and compliance. With features like EBR, audit trails, and electronic signatures, it streamlines production and ensures regulatory compliance while offering fast onboarding and cost-effective solutions.
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BatchLine Overview
BatchLine Lite MES is a modern manufacturing execution system designed for pharmaceutical and GxP-regulated companies. It digitizes and streamlines production, quality assurance, and compliance processes through automation and smart workflows. Core features include Electronic Batch Records (EBR), audit trails, user access control, and electronic signatures—enabling real-time data capture, compliance with FDA 21 CFR Part 11, and operational efficiency. With affordable pricing and rapid onboarding, BatchLine helps manufacturers of all sizes modernize operations and scale efficiently while meeting strict regulatory demands.
Features
Electronic Batch Records (EBR)
Audit Trails & Compliance Tools
User Access Controls & E-Signatures
Workflow Automation & Real-Time Analytics
BatchLine Pricing Overview
BatchLine Score
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FAQs
BatchLine Lite MES is a cloud-based Manufacturing Execution System tailored for GxP-regulated industries, offering electronic batch records, audit trails, and compliance tools to digitize production and quality processes.
BatchLine’s streamlined implementation process allows organizations to go live, validated, and operational with their first product within approximately 90 days.
Yes, BatchLine is designed to comply with FDA 21 CFR Part 11, EU Annex 11, and other GxP regulations, ensuring data integrity and audit readiness.
BatchLine supports integration with various systems, including ERP, LIMS, and manufacturing equipment, to streamline data flow and operations.
BatchLine provides ongoing support, including training, recipe design services, and customer service to ensure continuous operational excellence.
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