

Certivo
FDA 21 CFR Part 11 compliant electronic signatures for regulated industries like life sciences, pharma, and clinical trials.
Cost / License
- Subscription
- Proprietary
Platforms
- Online
- Software as a Service (SaaS)

Certivo
Features
- Audit Trail
Certivo News & Activities
Recent activities
Certivo information
What is Certivo?
Certivo is a secure electronic signature platform purpose-built for FDA 21 CFR Part 11 compliance. Unlike general-purpose e-signature tools, Certivo is designed from the ground up for regulated industries including life sciences, pharmaceuticals, biotech, and clinical trials.
Key features include TOTP-based two-factor authentication for every signature, immutable audit trails with 25-year retention, role-based access controls, and full traceability of document workflows. Certivo supports multi-signer workflows with configurable signing orders, real-time notifications, and a verification portal for third-party document validation.
The platform also covers EU Clinical Trial Regulation 536/2014, UK MHRA 2026, EU GMP Annex 11, and GDPR compliance requirements. It is delivered as a cloud-hosted SaaS solution with tiered pricing starting at $59.99/month for small teams, scaling up to enterprise plans with custom pricing.
