Speed up global drug and device launches with secure, validated translation management that meets FDA 21 CFR Part 11 and EU MDR standards. XTM's complete platform blends AI-powered translation with specialized tools for clinical trials, regulatory filings, and medical device localization.
With audit-ready tracking and enterprise-grade security, XTM Cloud ensures every document is accurate, compliant, and delivered on time—helping life sciences teams accelerate approvals and maintain patient trust.