Kivo

Kivo is a life sciences-focused software company that provides a unified platform for document management, quality management, and regulatory submissions. The company's flagship product, Kivo GO, is designed to streamline the drug development process by integrating Document Management (DMS), Quality Management (QMS), and Regulatory Information Management (RIM) into a single, user-friendly environment. Kivo specifically targets emerging biotech and pharmaceutical companies, offering tools for eCTD submissions, clinical trial master files (eTMF), and compliance with FDA 21 CFR Part 11. By automating workflows and centralizing data, Kivo helps smaller life science teams manage complex regulatory requirements more efficiently than traditional enterprise systems.