Loftware Cloud Compliance is the world’s first public, validation-ready cloud labelling solution. It is the simplest way to design and print labels in a regulated environment and often used within the pharmaceutical, medical devices and life sciences industries.

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Loftware Cloud Compliance can be used to digitise your entire approval process, automating mass label changes and approvals without creating hundreds of label variations and allowing you to test any changes before making them live in your production environment using the system’s three-tier environment: Development (DEV), Quality Assurance (QA) and Production (PROD)

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Loftware Cloud Compliance has been designed to comply with the major regulations impacting the life science industry, including EU MDR, FDA UDI, 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), plus a 12-year print history, which enables you to visually track every label you’ve printed during that time.

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Importantly, Loftware Cloud Compliance is a validation-ready labelling solution, designed to streamline the validation process, which is further enhanced with the option of the Validation Acceleration Pack (VAP). Our team can assist with IQ, OQ and PQ documentation as well. We also reduce the validation burden by only updating the software once a year and when it is time for a software release, we give you a three-month window before updating your production environment.