Giotto Compliance is an all-in-one platform to automatize, digitalize, and standardize the data collection, analysis and writing of a Clinical Evaluation Report. Our customers (MedTech companies worldwide) happily use Giotto Compliance to save an impressive amount of time and move into a digitalized and organized CER workflow with a strong automation component. OUR MISSION: Redefine how people and technology work together on the Clinical Evaluation of medical devices in the context of regulatory activities. OUR STORY: Giotto Compliance is developed and distributed by L2F SA, a Swiss technology company that was born in 2017 at the EPFL, one of Europe’s most vibrant science and technology institutions. Our AI-Based proprietary technology has been awarded multiple grants by the Swiss Innovation Agency and allowed us to win several eminent competitions worldwide, including Kaggle and Mindsphere. Giotto Compliance started as a simple AI-based tool for extracting data from medical publications, and has evolved over the years to become an All-in-One Platform to automatize, digitalize, and standardize the data collection, analysis and writing of a Clinical Evaluation Report.