Discover How to Streamline Medical Device Labeling and Artwork
In today’s highly regulated medical device landscape, labeling and artwork management isn’t just a compliance requirement, it’s a critical factor in ensuring patient safety, avoiding costly recalls, and maintaining brand integrity. This white paper explores the escalating challenges facing medical device manufacturers, from navigating FDA 21 CFR Part 11 and EU MDR/IVDR regulations to managing global consistency across thousands of SKUs. It outlines the operational pain points companies face, such as collaboration silos, manual proofreading errors, and inefficient approval workflows, as well as the risks they pose to compliance and speed-to-market.
The document also introduces Kallik's Veraciti, a purpose-built, cloud-native labeling and artwork management platform, built with highly regulated industries in mind. You’ll discover how its core capabilities, including centralized asset control, automated artwork generation, integrated AI proofreading, and real-time global collaboration, empower organizations to reduce errors, accelerate timelines, and achieve regulatory peace of mind. With a detailed comparison against leading competitors, the white paper makes a strong case for why Veraciti is the future-proof solution for medical device labeling.