Loftware Cloud Compliance

Labeling software

Validation-Ready Solution
World’s first public cloud labeling solution ready for validation in regulated environments.

12-Year Print History
Complete traceability of every label with visual tracking over 12 years.

Three-Tier Environment
DEV/QA/Prod for safe testing of changes before production.

Product information

Loftware Cloud Compliance is the world’s first public, validation-ready cloud solution for label design and printing in highly regulated sectors like life sciences. It solves challenges like complex approvals, validation issues, and traceability through digitized workflows, mass change automation, and compliance support.

It supports applications in pharma, medical devices, and chemicals with Label Designer, Application Builder, DMS featuring role-based access, versioning, configurable approvals, ERES, and integrations with databases, Excel, and ERP systems. Compatible with EU MDR, FDA UDI, 21 CFR Part 11, and EU GMP Annex 11, including 12-year print history and three-tier (DEV/QA/PROD) environments.

Validation is streamlined with the Validation Acceleration Pack (VAP), IQ/OQ/PQ documentation, and annual updates with a 3-month testing period. Codipack delivers Loftware Cloud Compliance as a partner solution, ideal for efficient, scalable labeling with ROI in under 6 months.

Specifications
  • Validation-ready with VAP, IQ/OQ/PQ support, and annual updates.
  • Compliance with EU MDR, FDA UDI, 21 CFR Part 11, EU GMP Annex 11.
  • Three-tier: Development (DEV), Quality Assurance (QA), Production (PROD).
  • Role-based access, Active Directory, OpenID Connect.
  • Document versioning, configurable approval workflows, ERES.
  • 12-year print history and analytics.
  • Label Designer and Application Builder for custom printing.
  • Integration with Access, Excel, 3rd party databases, web services.
  • Driverless printing from 3 printers, scalable.
  • 5GB document storage, test reports per release.

Frequently Asked Questions

Coding and labeling is our core business. We have 5000 customers in very diverse sectors: from the local cheese shop to the multinational.

Meets EU MDR, FDA UDI, FDA 21 CFR Part 11, and EU GMP Annex 11.

12 years print history for complete traceability.

Three-tier: DEV for development, QA for testing, PROD for live use.

VAP simplifies validation with documentation and streamlined processes.

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