High-Precision AI Translation for Clinical Research & Life Sciences

X-doc AI uses neural AI engines trained specifically on life sciences and clinical research terminology. For critical documents like Informed Consent Forms (ICFs) and Clinical Study Protocols (CSPs), we combine our 99% accurate AI with curated glossaries and optional human-in-the-loop review by subject-matter experts to ensure full accuracy and regulatory compliance.

Yes. Our platform is designed to handle complex regulatory submissions for global health authorities, including the FDA, EMA, and PMDA. We support eCTD formats and ensure that all translations meet the strict terminology, formatting, and compliance standards required for successful market access and regulatory affairs.

Our advanced AI analyzes and replicates the original document's layout, including complex tables, charts, graphs, footnotes, and multi-column formats found in CSRs and Investigator Brochures. For publication-ready quality, we offer an optional human typesetting service to guarantee a perfect match to the source document.

We provide enterprise-grade security to protect your most sensitive data. All translations are protected with end-to-end encryption, and our platform is certified for ISO 27001, SOC 2, and other leading security standards, ensuring compliance with data privacy regulations like GDPR and HIPAA.

Yes, we provide certified translations for official documents used in clinical trials that require legal validity. This includes investigator credentials, ethics committee approvals, patient medical records, and Certificates of Pharmaceutical Product (CPP), complete with a certificate of accuracy and official seal.