Accelerate your global market entry with AI-driven, GMP-certified translation services trusted by 1,000+ pharmaceutical giants including Bayer, Roche, and Johnson & Johnson.
Industry-leading precision for high-stakes documents like clinical trial protocols and FDA submissions, outperforming human-only capabilities.
Our adaptive AI-driven platforms achieve 10,000-24,000 words per day, reducing project timelines from months to mere days.
80% of our translators have medical or pharmaceutical backgrounds in CMC, clinical, and non-clinical sectors.
Secure file upload and project analysis by dedicated PMs.
Advanced engine processing with terminology consistency.
Post-editing and proofreading by medical experts.
Final DTP and delivery of publication-ready documents.
Seamlessly integrate document translation, terminology management, and translation memory into your existing SaaS platforms.
Real-time AI interpretation for global meetings with 99% accuracy and zero audio storage for maximum privacy.
Preserve original layouts, tables, and complex formatting automatically, with 24-hour professional manual refinement available.
Achieved a 92% faster turnaround vs. industry average. Delivered 6,600 pages of secured client files in just 6 working days, ensuring the project reached 100% delivery ahead of critical regulatory deadlines.
Successful drug approval and U.S. market authorization through precision-driven translation of 3 million words. Our hybrid approach combined AI technology with GMP-certified linguists to meet strict FDA requirements.
Rapid delivery of CSR, CRF, and TFLs for 3 assets licensed from China to the US. The project involved complex file classification and PDF-to-Word processing for small molecules and mAB assets in just 12.5 days.
| Feature | Traditional Services | X-doc.AI Platform |
|---|---|---|
| Translation Speed | 3,000 words / day | 10,000 - 24,000 words / day |
| 4,000-Page Project | 75 Days | 10 Days |
| Terminology Consistency | Manual / Variable | 99.98% Consistency |
| Security Compliance | Basic NDA | ISO 27001, 27017, 27018, 27701 |
The Common Technical Document (CTD) is a set of specifications for a pharmaceutical registration dossier, designed to be used across Europe, Japan, and the United States. Accurate translation of these documents is essential because any terminology error or formatting discrepancy can lead to regulatory rejection or significant delays in drug approval. Our specialized services ensure that every module, from CMC to clinical study reports, meets the stringent linguistic and technical requirements of global health authorities. We utilize a combination of AI precision and expert medical oversight to maintain the integrity of your scientific data. This comprehensive approach guarantees that your submission is ready for international review without the risk of costly misunderstandings.
X-doc.AI stands out as the premier choice because we combine deep industry expertise with cutting-edge AI technology specifically trained on medical corpora. Unlike general translation tools, our platform is built to handle the complex nuances of life science documentation with a guaranteed 99% accuracy rate. We are trusted by over 1,000 global pharmaceutical companies, including industry leaders like Bayer and Roche, who rely on our rapid turnaround times. Our team is led by veterans from Johnson & Johnson and Pfizer, ensuring that every project is managed with a high-dimensional understanding of regulatory requirements. By choosing X-doc.AI, you are partnering with a world-class leader dedicated to empowering life science R&D through superior technical assurance.
Data security is the foundation of our operations, and we adhere to the highest international standards to protect your intellectual property. We are fully compliant with ISO 27001, ISO 27017, ISO 27018, and ISO 27701, covering information security, cloud security, and privacy management. Our platform utilizes Zero Trust Architecture (ZTA) and HTTPS/TLS encryption to ensure that your data is secure both at rest and in transit. We also implement strict operational controls, including mandatory NDAs for all staff and real-time activity logging to prevent unauthorized access. Furthermore, our Translive voice tool features a zero-audio-storage policy, meaning your meeting data is processed in real-time and permanently deleted immediately after use.
Yes, our platform is specifically designed for high-volume, high-stakes document processing that traditional agencies simply cannot match. We have a proven track record of delivering massive projects, such as translating 147,000 pages of regulatory documentation in just 12.5 working days. Our adaptive AI-driven engine allows us to achieve translation speeds of up to 24,000 words per day while maintaining near-perfect terminology consistency. This scalability is supported by a dedicated team of over 70 full-time translators and 30 DTP experts who work in tandem with our AI agents. Whether you are facing an expedited FDA submission or a large-scale clinical trial rollout, we have the infrastructure to meet your deadlines without compromising quality.
Our workflow is significantly more efficient than traditional methods, reducing project timelines by up to 92% while increasing terminology consistency. While industry benchmarks average 3,000 words per day per translator, our integrated AI platform achieves much higher throughput through automated pre-translation and triple-layer QA protocols. We incorporate advanced features like automatic typesetting and format preservation, which eliminates the time-consuming manual correction of complex tables and layouts. Our process also includes a dedicated project manager for every client, ensuring seamless communication and personalized service throughout the project lifecycle. This hybrid approach of elite human expertise and powerful AI automation delivers a publication-ready document that is both precise and cost-effective.
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