Kivo

Kivo provides a unified, cloud-based compliance and document management workspace for clinical-stage biotech teams and their service partners. The Kivo platform is a CSA-validated shared environment in which Regulatory, Clinical, and Quality teams manage documents, activities, vendors, submissions and trial records in one place. Controlled workflows, audit trails, version history and electronic signatures are built into the system.

The company's technical work spans cloud-based software, regulated document management, compliance workflows and enterprise collaboration. Its stated aim is to make compliance less complicated, designing around how smaller life science organisations actually work rather than imposing heavyweight enterprise processes. The platform is also intended to support distributed teams and partners that change over time.

Work at Kivo is organised around close cooperation between regulatory specialists, software builders, implementation teams and customers. The approach is domain-led and practical, with regulatory experts and software architects working together, and cross-functional implementation and customer partnership treated as central to delivering lasting operational value. The company describes customer success as the measure of its own.

Kivo operates in the biotech (clinical-stage), life sciences, clinical trials, regulatory affairs, quality management and pharmaceutical services sectors. Further information is available at https://kivo.io/.