Liqvor Pharmaceutical Selects Bever to Implement Manufacturing Management System on Dynamics 365

Implementation of a Microsoft Dynamics 365–based manufacturing and quality management platform for a pharmaceutical production company. The system supports daily operations across production, quality assurance, regulatory documentation, finance, and supply chain departments, and serves as a centralized operational backbone for manufacturing and compliance processes.

Manufacturing & Product Dossier Management

• Automatic generation of pharmaceutical manufacturing dossiers
• Registration of chemical and biological laboratory test results
• Recording production parameters (autoclave data, temperature, mixing speed, batch conditions)
• Bulk product property tracking per batch
• Packaging data and batch traceability
• Centralized storage of all production and quality documentation required for regulatory audits

Quality Management (CAPA & SOP)

• CAPA (Corrective and Preventive Actions) case registration and tracking
• Root cause analysis workflows and approval processes
• SOP document lifecycle management (creation, approval, versioning, expiry)
• Deviation and non-conformance tracking
• Audit preparation and compliance monitoring

Financial Analysis & Costing

• Unit cost calculation based on raw materials, labor, and production overhead
• Batch profitability analysis
• Profit & Loss reporting
• Production cost comparison across batches and products
• Financial analytics dashboards for management decision-making

Supply Chain & Inventory Operations

• Vendor and supplier management
• Purchase order lifecycle management
• Raw material receiving and quality checks
• Warehouse inventory tracking and batch/lot traceability
• Stock consumption tracking during production

Operational Efficiency & Compliance

• Centralized data model connecting production, quality, and finance
• Full product genealogy from raw material to packaged product
• Faster audit preparation through structured documentation
• Reduced manual documentation and spreadsheet usage
• Improved regulatory compliance and operational transparency

This implementation transformed previously manual and document-heavy pharmaceutical processes into a structured digital workflow, improving traceability, compliance readiness, and cost visibility across the manufacturing lifecycle.