You can use Kivo to manage regulatory documents, quality systems, and clinical trial records in one secure place. The system combines document management, regulatory submission tracking, electronic trial master files, and quality event management for biotech and pharmaceutical companies. Teams can collaborate in real time using Microsoft Office tools, request electronic signatures compliant with FDA regulations, and track approvals with automated audit trails. Kivo also handles software validation automatically, letting life sciences teams run audits, oversee clinical trials, and file regulatory submissions without maintaining complex infrastructure.
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