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Klyverity is a compliance-focused electronic signature platform designed for clinical trials, pharmaceuticals, life sciences, and other regulated industries. It supports secure document signing workflows for PDFs, including the ability to upload documents, add signature fields, assign signers, and track signing progress through completion.
The platform is built around regulatory requirements such as FDA 21 CFR Part 11, EU CTR 536/2014, GDPR, and EU GMP Annex 11. It includes audit trails, validation documentation, configurable access controls, and long-term document retention designed for regulated recordkeeping needs. Klyverity also supports sequential and parallel signing, deadline reminders, regulatory exports, and secure signing links for recipients who do not need an account.
Security features include two-factor authentication, encrypted data handling, and audit logging for signature events. The app is suited for organizations that need compliant electronic records, controlled signing workflows, and traceable document management for clinical and quality-related processes.
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