Inspection-Ready Documentation
Automatically generated compliance reports, access logs, and change histories provide a single source of truth for regulators. Verixa centralizes your validation and usage evidence, saving teams hundreds of hours of manual prep.
Guided Prep for FDA/EMA Inspections
Verixa includes tailored checklists and readiness tools to support FDA and EMA regulatory requirements. Whether it's an announced inspection or a surprise visit, our system ensures that all necessary records are up to date, traceable, and easily retrievable.
Collaboration with QA & RA Teams
We work hand-in-hand with your Quality Assurance and Regulatory Affairs teams to customize validation documentation, align to internal SOPs, and ensure continuous compliance across all projects.
Verixa transformed our audit preparation process. What used to take weeks now takes days, and our last FDA inspection went smoother than we could have imagined.
Our compliance experts empower life sciences teams to confidently prepare for FDA, EMA, and global regulatory audits.
Company approach
Through AI-powered chatbots and recommendation engines, we ensure your customers receive personalized experiences that boost retention and conversion.
Audit Readiness
Verixa streamlines compliance and regulatory prep through centralized audit logs, role-based controls, and automated report generation. Our tools help you stay inspection-ready with documentation tailored for FDA, EMA, and other regulatory bodies—ensuring you're always prepared, never scrambling.