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ERP for Pharmaceutical Industry Compliance Needs

Pharma ERP software is designed to meet the specific needs of pharmaceutical manufacturers and distributors. It helps in managing key areas like formulation, production, batch tracking, quality checks and regulatory compliance. With features like expiry date tracking, audit logs and easy reporting, it reduces manual work and improves accuracy. It also gives better visibility across departments, so teams can make faster and smarter decisions.

    Bullet point arrow for Batch Production & Quality Management
  • Batch Production & Quality Management
  • Bullet point arrow for Regulatory Compliance & Documentation
  • Regulatory Compliance & Documentation
  • Bullet point arrow for Inventory & Expiry Management
  • Inventory & Expiry Management
  • Bullet point arrow for Sales, Distribution & GST Accounting
  • Sales, Distribution & GST Accounting
  • Bullet point arrow for Purchase & Supplier Control
  • Purchase & Supplier Control
Batch Production & Quality Management icon

Batch Production & Quality Management

Automate production processes with real-time batch tracking, standard operating procedures and integrated QA checks

  • Formula-Based Batch Manufacturing feature checkmark
    Formula-Based Batch Manufacturing
  • BMR, BPR and SOP Integration feature checkmark
    BMR, BPR and SOP Integration
  • Quality Inspection & Lab Analysis feature checkmark
    Quality Inspection & Lab Analysis
Inventory & Expiry Management icon

Inventory & Expiry Management

Track raw materials and finished goods with multi-level inventory control and automatic expiry alerts.

  • Batch-Wise Inventory Control feature checkmark
    Batch-Wise Inventory Control
  • Expiry & Reorder Notifications feature checkmark
    Expiry & Reorder Notifications
  • Cold Chain & Hazardous Stock Handling feature checkmark
    Cold Chain & Hazardous Stock Handling

Frequently Asked Questions

Pharma ERP software helps manage and automate key processes such as production, inventory and compliance to improve accuracy and ensure regulatory alignment.

Yes, it includes batch processing capabilities with complete traceability, from raw material sourcing to final product distribution.

Yes. It enforces formula versioning with approvals and audit logs, provides electronic batch and weigh tickets, sample testing plans, non‑conformance logging, CAPA workflows, COA/MBR/BMR creation and electronic signatures compliant with FDA 21 CFR Part 11 and similar regulations

Industry Information

  • Industry:
    Pharmaceutical
  • Solution:
    Integrated Pharmaceutical Manufacturing System
  • Modules:
    Production Control, Quality Management, Document Control, Regulatory Compliance, R&D Management
  • Result:
    45% faster batch release time, 40% reduction in compliance costs, 35% improvement in quality metrics
  Pharmaceutical Manufacturing Guide preview