Klyverity Reviews & Product Details

Klyverity is a cloud-based electronic signature platform purpose-built for FDA 21 CFR Part 11 compliance. Designed for regulated industries including clinical research, pharmaceutical, biotech, medical device, and life sciences teams, Klyverity ensures every signature meets strict regulatory requirements out of the box. Key features include TOTP-based two-factor authentication, ALCOA+ audit trails with SHA-256 hash-chain verification, RFC 3161 trusted timestamps, and a verifiable Certificate of Completion for every finished envelope. The platform supports multi-signer workflows with role-based field placement, real-time signing status tracking, secure guest signing with no account required, and a public verification portal for third-party document validation. Klyverity eliminates the compliance gaps found in general-purpose e-signature tools. Teams can upload documents, assign signature fields, collect legally binding signatures, and generate complete audit trails, all within a single platform designed from day one to satisfy FDA 21 CFR Part 11, ESIGN, UETA, and eIDAS requirements for regulated industries. The platform is delivered as a multi-tenant SaaS solution hosted securely in the cloud. It offers tiered pricing to accommodate teams of all sizes, from small research groups to enterprise organizations, with a 14-day free trial and compliance documentation included with all plans. Klyverity requires no on-premise infrastructure or complex IT setup, enabling teams to begin collecting compliant electronic signatures within minutes of account creation. (Klyverity was formerly known as Certivo.)