Klyverity is an e-signature platform purpose-built for regulated industries. Every signature is backed by an ALCOA+ audit trail with SHA-256 hash-chain verification, an RFC 3161 trusted timestamp, and a verifiable Certificate of Completion, so the proof holds up to an FDA inspection. Compliant with FDA 21 CFR Part 11, ESIGN, UETA, and eIDAS. Built for clinical research, pharma, biotech, and medical device teams.
Certivo is an electronic signature platform purpose-built for regulated industries — clinical trials, pharma, medical devices, and life sciences. Unlike general-purpose e-signature tools, every feature is designed around FDA 21 CFR Part 11 compliance from the ground up. Features include ALCOA+ compliant audit trails with hash-chain verification, 25-year document retention, workflow automation, role-based access control, and built-in MFA. Compliant with FDA, EU CTR 536/2014, MHRA 2026, and GDPR.
