The pharmaceutical industry works under some of the most demanding regulatory, quality, and safety standards. Manufacturers must handle precise formulations, controlled environments, batch production, validation, documentation, and real-time traceability across every stage from raw material sourcing to final packaging. Managing production schedules, QC testing, equipment sterilization, documentation, and compliance manually increases risk, delays approvals, and reduces overall efficiency.
eresource Bpro ERP is built specifically for pharmaceutical companies, bulk drug manufacturers, API producers, formulation units, and contract manufacturers. It integrates formulation management, batch processing, validation, quality control, warehouse management, supply chain, and finance into a unified, compliant platform.
The system supports tablets, capsules, syrups, injectables, ointments, powders, APIs, intermediates, and bulk drugs. With digital batch records, controlled workflows, and compliance-ready documentation, manufacturers can maintain consistency, meet global regulatory standards, and ensure safe, high-quality production.
With real-time visibility, automated workflows, and strict traceability, eresource Bpro helps companies eliminate manual errors, shorten production cycles, and maintain unmatched regulatory compliance across all operations.