Verixa supports the industry-standard Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) model. This ensures that the platform is not only installed correctly and functions as intended, but also performs consistently under real-world conditions. Validation documentation and protocols are readily available to support customer-specific qualification efforts.

Full traceability is embedded into the system architecture. From user actions to configuration changes, every interaction is logged and available for audit. Evidence collection is streamlined, providing a clear and compliant chain of custody that simplifies quality assurance and regulatory submissions.

Verixa is architected with compliance to 21 CFR Part 11 in mind, ensuring secure, validated electronic records and signatures. Role-based controls, audit trails, and e-signature authentication workflows are built-in, supporting FDA-aligned digital recordkeeping practices.