Launching Soon

Precision ERP for
Medical Device
Manufacturing.

A comprehensive, compliance-first ERP system designed for MedTech innovators. Streamline your entire lifecycle from raw materials to final release with built-in ISO 13485 & CDSCO logging.

Built for CDSCO & ISO 13485 compliance.

Generating Dashboard Preview...

End-to-End Control Modules

Purpose-built modules to manage every critical touchpoint of your medical manufacturing process without the bloat of generic ERPs.

Manufacturing (eDHR)

Digitize your production floor. Manage Bill of Materials (BOM), complex routings, and work orders. Automatically generate electronic Device History Records (eDHR) to ensure every manufactured unit is fully traceable.

  • Automated eDHR compilation
  • Real-time Work Order tracking
  • Multi-level BOM management

Stores & Inventory

Strict inventory controls critical for medical devices. Manage raw materials, work-in-progress, and finished goods with rigid Quarantine and Released statuses to prevent unauthorized usage.

  • Quarantine/Release state enforcement
  • Expiry & FIFO tracking
  • End-to-end batch & lot traceability

Quality Control (QC)

Digitize inspection logs to eliminate paper errors. Handle incoming material inspections, in-process checks, and final product approvals. Integrated Non-Conformance (NC) workflows.

  • Standardized Inspection Plans
  • Automated AQL Sampling
  • Non-Conformance (NCR) generation

Quality Assurance (QA)

Maintain total oversight of your Quality Management System (QMS). Connect CAPAs directly to manufacturing anomalies and manage document versions seamlessly.

  • Integrated CAPA management
  • Document Control & Training matrices
  • Internal Audit scheduling

Compliance is not an afterthought. It's built-in.

Medico ERP eliminates the panic of regulatory audits. Every action, status change, and approval is logged securely to ensure continuous compliance with Indian and international medical device regulations.

ISO 13485 Data Logging

Enforced workflows guarantee that QMS procedures are followed before any batch is released.

CDSCO Audit Trails

Detailed, immutable logs mapping out 'who, what, and when' to satisfy stringent CDSCO inspectors.

21 CFR Part 11 Signatures

Secure electronic signatures and multi-factor authentication for critical quality approvals.