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Manufacturing Execution System (MES / eBMR)

Pharma MES Software — Digital Manufacturing Platform for GxP Compliant Batch Manufacturing Automation

AmpleLogic is a purpose-built pharma MES software and pharmaceutical manufacturing software — a life sciences MES platform and digital manufacturing platform delivering shopfloor execution system, GMP manufacturing software, cloud MES platform, AI-driven manufacturing insights, electronic batch manufacturing, weighing scale integrations, recipe management, real-time production monitoring, EE monitoring, batch manufacturing automation, and smart factory platform for pharma manufacturing digitalization.

keyFeatures

everythingYouNeed

Electronic Batch Manufacturing

Electronic batch manufacturing with paperless batch manufacturing automation, step-by-step guided execution, and real-time verification on this pharma MES software.

Weighing Scale Integrations

Weighing scale integrations with barcode verification, automatic calculations, and digital manufacturing platform data capture.

In-Process Controls

Real-time production monitoring of critical process parameters with automatic alerts and EE monitoring for deviations.

Equipment Integration

Shopfloor execution system with direct integration to shop floor equipment for automatic data capture on this GxP compliant MES.

Review by Exception

AI-driven manufacturing insights with automated review workflows highlighting only exceptions for faster batch release.

Recipe Management

Recipe management with drag-and-drop master recipe creation, version control, and low-code manufacturing applications.

benefits

whyChoose

Reduce batch release time by 50% with this pharma MES software
Eliminate right-first-time errors with batch manufacturing automation
Real-time production monitoring visibility across the digital manufacturing platform
Automated deviation detection via AI-driven manufacturing insights
Paperless manufacturing floor through pharma manufacturing digitalization
Faster regulatory audits with GxP compliant MES

complianceStandards

builtForCompliance

USFDA 21 CFR Part 11EU Annex 11GMPGAMP 5ICH Q7

useCases

designedForWorkflows

Batch ManufacturingContinuous ManufacturingPackaging OperationsAPI ManufacturingBiotech Production

readyToTransform

ctaDescription

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