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Overview
POMS MES delivers a specialized execution system for regulated industries, enabling paperless batch records to accelerate quality review. Despite some user reports of ‘slowness’, the software’s pre-validated, configurable modules and strong support team make it a trusted choice for cGMP compliance.
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Starting Price
Custom
POMS MES Specifications
Inventory Management
Quality Control
Work Order Management
Real-Time Monitoring
What Is POMS MES?
POMS MES is a specialized Manufacturing Execution System designed for regulated industries like pharmaceuticals, biotechnology, and life sciences. It directly addresses cGMP compliance challenges by replacing paper-based processes. It delivers a comprehensive paperless Electronic Batch Record (EBR) solution, enabling streamlined quality reviews through ‘Release-By-Exception', which accelerates product release and improves operational consistency.
POMS MES Pricing
POMS MES Integrations
Who Is POMS MES For?
POMS MES is ideal for a wide range of industries and sectors, including:
- Pharmaceutical
- Biotechnology
- Medical device
- Consumer packaged goods
- Life sciences
Is POMS MES Right For You?
POMS MES is not a general-purpose solution; it is an enterprise-grade platform for manufacturers where cGMP compliance is paramount. Its standout capability, ‘Release-By-Exception', offers a direct path to accelerating quality review and shortening cash cycles. This specific focus on solving the challenges of paper-based regulated manufacturing has earned the POMS MES software great customer satisfaction. If your organization struggles with paper batch records and delayed releases, the software is a compelling choice.
Are you still not sure about POMS MES and need expert advice to make an informed decision? Reach out to us at (661) 384-7070 now.
POMS MES Features
The system’s EBR module captures all processed information, data, and events during the manufacturing process and quality review. This consolidates critical production data into a single, comprehensive source, eliminating paper records and supporting paperless operations.
This module specifies and controls all materials, including raw, intermediate, and finished goods. It manages material movement, reports waste, and adjusts inventory in real-time, supporting both lot-level and container-level tracking for full integrity.
This module manages all specifications required to implement a proposed solution. It is described as the heart of the recipe authoring process and includes crucial functions like version control and effectivity dating for all objects.
This functionality is designed to automate and simplify regulatory compliance. It enforces cGMP practices locally or globally and manages critical quality goals like expiry dating, retesting, horizon policies, and lot disposition.
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