Certivo
FDA 21 CFR Part 11 compliant electronic signatures
Certivo launched on March 16, 2026 with 5 votes, #1,928 of 23,380 launches that month and more than 75% of that year's launches.
What it does
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.
Klyverity is purpose-built for FDA 21 CFR Part 11 and GxP compliance. Legally binding e-signatures with ALCOA+ audit trails, 2FA, and 25-year retention.
The secure e-signature platform built for clinical trials, pharmaceuticals, and life sciences. Purpose-built for FDA 21 CFR Part 11 and EU CTR 536/2014, with hash-chained audit trails, GDPR support features, and configurable retention policies. Upload your PDF document and add signature fields, initials, dates, and custom form fields. Add recipients with sequential or parallel routing. Set signing order and deadline reminders. Monitor signing progress in real-time. Download signed documents with complete audit trails. Part 11 controls with validation documentation, IQ/OQ protocols, and configurable settings. Immutable hash-chain audit trails capturing who, what, when, where, and why for…from klyverity.com
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