Pivot-MES is Pivot Path’s modular Manufacturing Execution System (MES) designed for pharmaceutical manufacturers seeking enterprise-grade compliance without the complexity, cost, or lengthy implementation timelines of traditional MES solutions. Built on a validated technology foundation, Pivot-MES helps manufacturers digitize shop floor operations, improve production visibility, strengthen data integrity, and maintain continuous GxP compliance.
The platform enables organizations to start with eLogbooks, replacing paper-based equipment, room, and activity records with digital, audit-ready workflows, and then scale to Electronic Batch Manufacturing Records (eBMR) and Electronic Batch Processing Records (eBPR) as requirements evolve. Key capabilities include guided task execution, electronic data capture, process interlocks, exception and deviation reporting, real-time workflow management, and comprehensive audit trails. Built-in controls help prevent out-of-sequence activities, missing approvals, and data integrity issues while ensuring traceability throughout manufacturing operations.
Pivot-MES integrates seamlessly with ERP systems such as SAP, PLC/SCADA equipment, manufacturing instruments, historians, and data lakes, creating a connected digital manufacturing environment. Designed for rapid deployment, organizations can go live within weeks without requiring a dedicated IT or OT team. The platform is aligned with GxP, 21 CFR Part 11, and EU Annex 11 requirements, helping manufacturers improve efficiency, reduce manual errors, enhance compliance, and accelerate digital transformation across production operations.
