A leading automation solutions provider for the pharmaceutical industry, offering a visual, drag-and-drop development platform with an intuitive interface and 36 data components for data verification and validation, shortening application development time. Its 21 CFR Part 11-compliant and EU Annex 11 solutions are in use at more than 17 US FDA, 3 MHRA and 10 WHO-approved units. By adapting the traditional V-model with a configuration and experimentation phase, AmpleLogic accelerates GMP automation and addresses data integrity issues related to revalidation, deviations and release management, reducing implementation time by 70%, and has built 14 ready-to-use apps for QA, QC and production.
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