Label Cloud Compliance
for
Pharmaceutical & Medical Devices
Manufacturers

The simplest way to design and print labels in a regulated environment. Label Cloud Compliance is the world's first, public validation-ready Cloud labelling solution. It enables all businesses, of any size, manage labelling in a Pharma or Medical Devices regulated environment.

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Features:

  • Digitise and standardise the label approval process, eliminate labelling errors and remove the need for manual quality assurance procedures. Label Cloud Compliance features a three-tier environment; Development (DEV), Quality Assurance (QA) and Production (PROD), so you can test any changes before making them live in your production environment.

  • Automate mass label changes and approvals, without creating hundreds of label variations.

  • Capture and trace every label printed with records being stored for up to 12 years.

  • When it’s time for a new software release, NiceLabel give you a three-month window before updating your production environment. You get the benefits of a continuously updated and maintained labeling solution, without increasing the validation workload on your IT staff.

  • Simplify compliance with industry specific regulations, incuding FDA UDI, EU MDR, FDA 21 CFR Part 11 and EU GMP Annex 11. It includes built-in role-based access, document versioning, configurable approval workflows, electronic records and electronic signatures (ERES).

  • Remove delays caused by the validation process using the tools already set-up within Lable Cloud Compliance. Our team takes care of the IQ documentation, and can assist with OQ and PQ as well. We also reduce the validation burden by only updating the software once a year.

  • Easily scale a compliant labelling solution to multiple sites, countries and business partners, to avoid costly errors within the supply chain.
     

Interested in finding out more about Label Cloud Compliance and the benefits for your business? Contact us for a demonstration.