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Medical Device Master
Centralized device, component and material records with controlled specifications and approvals.
Manage medical device components, material traceability, production batches, quality inspections, inventory, costing, and MDR regulatory compliance documentation.
Key capabilities
Keep commercial, manufacturing and quality data connected throughout the product lifecycle.
Centralized device, component and material records with controlled specifications and approvals.
Manage product designs, technical specifications, revisions and documentation.
Track suppliers, incoming materials, stock levels and material traceability.
Maintain production orders, manufacturing records and batch traceability.
ATrack device identification, UDI details, batch or serial numbers and distribution records.
Maintain regulatory documents, risk records, compliance evidence and audit trails.
Integrate product costing, inventory valuation, sales, invoicing and financial accounts.
Ensure quality with digital management
Maximize equipment uptime efficiently
Simplify global regulatory compliance
Automate HR and payroll operations
Manage leads, customers, and sales
All financial reports in single page
Real-time dashboards and business insights
All compliance documents
From your website to direct order in ERP
2D barcodes and QR codes
e-BMR, e-SOP
Discover how Pharmacomputer ERP streamlines production, QA/QC, inventory, finance, and regulatory compliance.
Manage material, production, testing, traceability, inventory and FSSAI-oriented records.