Kivo builds cloud-based software for clinical-stage biotech teams and their service partners. Its compliance workspace platform gives Regulatory, Clinical, and Quality functions a single shared environment for managing documents, activities, vendors, submissions and trial records. The platform is CSA-validated and provides controlled workflows, audit trails, version history and electronic signatures to support work on regulated documents and processes.
The technical work spans document management, regulated workflow automation, audit trails and version control, and electronic signatures, delivered as cloud-based software. The product is designed around how smaller life science organisations actually operate rather than around heavyweight enterprise processes, with support for distributed teams and changing partners.
Development is shaped by close cooperation between regulatory specialists, software architects, implementation teams and customers. Regulatory experts and software builders work together on a domain-led approach, and cross-functional implementation and customer partnership are central to how the company delivers and sustains its platform. Customer success is described internally as the measure of the company's own success.
Kivo operates in the life sciences, pharmaceutical and clinical trials sectors.
