Translate Pharmaceutical Regulatory Documents with Confidence

Bluente's layout-aware engine specifically preserves complex structures like tables, charts, footnotes, legal numbering, and styles across all document formats (PDF, DOCX, PPTX, XLSX). Our technology was designed to maintain pixel-perfect layout retention, ensuring that regulatory submissions maintain their exact original formatting—a critical requirement for health authority submissions where formatting errors can cause delays or compliance issues.

Bluente supports all common document formats used in pharmaceutical regulatory submissions, including PDF, DOCX, PPTX, XLSX, and images (JPG/PNG/TIFF). Our platform also handles XML, JSON, TXT, and CSV files. For scanned regulatory documents, our advanced OCR technology converts non-selectable text into editable, searchable, and translatable content while maintaining the original document structure.

Bluente provides enterprise-grade security with encryption and automatic file deletion. We understand pharmaceutical regulatory documents contain highly confidential information about drug development, clinical trials, and proprietary processes. Our platform is built with security as a priority, ensuring your sensitive regulatory materials remain protected throughout the translation process.

Bluente translates large regulatory documents and multi-document batches within minutes, not days. This rapid processing is essential for time-sensitive workflows like drug approval processes and regulatory submissions. The platform scales to handle extensive documentation packages common in pharmaceutical regulatory environments.

Yes, Bluente generates bilingual outputs with side-by-side originals and translations, enabling quick comparative review—vital for regulatory accuracy verification. For documents with tracked changes or comments, these elements are preserved in the translation, supporting collaborative review processes common in pharmaceutical regulatory submissions.

Bluente supports translation across 120+ languages, covering all major languages required for global pharmaceutical regulatory submissions. This extensive language support ensures pharmaceutical companies can prepare documentation for health authorities worldwide without needing multiple translation providers.

Yes, Bluente's advanced OCR technology specifically converts non-selectable text in scanned PDFs and images into editable, searchable, and translatable content. This is particularly valuable for older regulatory documentation, certificates of analysis, or archived submissions that may only exist as scanned copies while still requiring accurate translation.