Kallik Veraciti™ is a fully integrated, cloud-native enterprise platform designed for end-to-end labeling and artwork management, primarily serving highly regulated industries like pharmaceuticals, medical devices, chemicals, cosmetics, and food & beverage. The platform's core value proposition is to provide a single source of truth for all product packaging assets, driving total regulatory compliance and accelerating time-to-market by up to 70%.
Key Features and Capabilities:
- Automated Artwork Generation (AAG) & Rules Engine: The system automatically assembles pre-approved content into labels and artworks using an Advanced Rules Engine, eliminating manual errors and drastically reducing project completion times from days to seconds.
- Asset & Phrase Management: Centralizes all content, data, icons, symbols, and translations in one auditable location, ensuring global consistency and easy reuse across thousands of labels. The "Where Used" functionality allows for instant identification and update of every affected label when a change occurs.
- Compliance & Audit Trails: Veraciti is built to ensure compliance with stringent regulations (e.g., FDA 21 CFR Part 11, EU MDR) by providing full audit trails, version control, e-signatures, and customizable role-based digital approval workflows.
- AI-powered Digitization (AToM): The AI-powered AToM tool rapidly speeds up data and content take-on, helping organizations onboard faster and migrate legacy artwork and labels into the new system.
- Factory Print Management (PCV): The platform extends to the factory floor with features like Print Count Validation (PCV) and three print options (Manual, Integrated, Direct Print) to ensure labeling hierarchy, accuracy, and traceability during the manufacturing process.
- Deployment: Delivered as a highly configurable Software as a Service (SaaS) platform, hosted securely on Amazon Web Services (AWS) for maximum scalability and security.
Target Users and Use Cases:
Veraciti is specifically designed for large, global enterprise organizations in highly regulated sectors. Primary use cases include managing complex, multilingual labeling requirements, ensuring adherence to global regulatory standards (like EU MDR and FDA regulations), and streamlining operations during business events such as mergers and acquisitions.