High-Precision AI Translation for Pharmaceutical & Life Sciences

X-doc AI uses domain-trained neural engines specifically for medical, clinical, and regulatory content. Our system leverages curated glossaries and terminology databases to achieve over 99% accuracy on industry-specific lexicons, ensuring that terms in documents like Clinical Trial Protocols, MAAs, and scientific papers are translated consistently and correctly.

Yes. Our platform is designed for regulatory compliance. We support formats like eCTD and provide certified translations with full audit trails. Our service combines AI efficiency with optional human-in-the-loop validation from accredited linguists to meet the stringent requirements of health authorities like the FDA, EMA, and PMDA.

We specialize in localizing all clinical trial documentation, including Informed Consent Forms (ICFs), patient recruitment materials, and investigator brochures. Our platform ensures terminology is consistent across all documents and languages, which is critical for multinational trials, patient safety, and data integrity.

Absolutely. Our layout-preservation technology intelligently analyzes and replicates the original document's structure, including tables, charts, multi-column layouts, and footnotes. This is essential for Instructions for Use (IFUs) and Patient Information Leaflets (PILs), eliminating manual rework and ensuring the final document is clear and compliant.

We provide enterprise-grade security for all translations. Our platform features end-to-end encryption, secure API integration, and is certified with ISO 27001, SOC 2, and other standards. This ensures that your confidential R&D data, patient information, and intellectual property are protected throughout the translation process, in line with GDPR and HIPAA requirements.