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Klyverity

FDA 21 CFR Part 11 compliant electronic signatures for regulated industries like life sciences, pharma, and clinical trials.

Dashboard: workspace overview of workflows, templates, and team activity

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  • Subscription
  • Proprietary

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  • Online
  • Software as a Service (SaaS)
Certificate of Completion with signer identity, SHA-256 hash, and RFC 3161 trusted timestamp
Public document verification: anyone can confirm a signed document is authentic
+3
ALCOA+ audit trail: every action logged with hash-chain verification (21 CFR Part 11)
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Klyverity was added to AlternativeTo by Klyverity on and this page was last updated .
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What is Klyverity?

Klyverity is a secure electronic signature platform purpose-built for FDA 21 CFR Part 11 compliance. Unlike general-purpose e-signature tools, Klyverity is designed from the ground up for regulated industries including life sciences, pharmaceuticals, biotech, and clinical trials.

Every signature captures the signer's identity, intent, and a trusted timestamp, then resolves into verifiable evidence: a tamper-evident SHA-256 hash-chain audit trail, an RFC 3161 trusted timestamp, and a Certificate of Completion that anyone can verify. Key features include TOTP-based two-factor authentication, ALCOA+ audit trails, role-based access controls, multi-signer workflows with configurable signing orders, secure guest signing with no account required, and a public verification portal for third-party document validation.

Klyverity is compliant with FDA 21 CFR Part 11, ESIGN, UETA, and eIDAS.

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