Translate Clinical Trial Documentation, Submission-Ready
Translate clinical trial documentation while preserving exact layouts. Bluente ensures patient consent forms and protocols maintain full integrity for regulatory acceptance.
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Clinical Trial Document Translation Made Simple
Clinical trial documentation requires meticulous translation that preserves every detail for regulatory approval. Generic translation tools often break critical formatting, creating compliance risks and lengthy rework.
Bluente's AI-powered platform is specifically designed to handle complex clinical trial materials with precision. Our format-perfect translation maintains original layouts, tables, charts, and legal numbering across all your PDF, DOCX, PPTX, and XLSX files.
Advanced OCR capabilities transform even scanned consent forms into editable, translatable content while preserving structure. Generate side-by-side bilingual outputs for efficient review and ensure data integrity with enterprise-grade security and encryption.
Cut turnaround time from days to minutes while maintaining the exact formatting regulatory bodies require for submission-ready documentation.
What's included in our instant document translation?
Bluente gives you fast, secure, and scalable access to high-quality translations across 120+ languages for your documents.
Our advanced terminology recognition and layout preservation deliver exceptional accuracy, trusted by legal and finance professionals who require precision.
Instant Document Translation
Fast, reliable document translation for seamless workflows.
- 120+ languages
Comprehensive language coverage for global reach
- Multi-format support: PDF, DOCX, PPTX, XLSX, images
Translate all your document types
- Layout-aware engine
Preserves tables, charts, footnotes, numbering, and styles
- Advanced OCR for scanned documents
Convert non-selectable text into editable, searchable content
- Bilingual and review-ready outputs
Side-by-side originals/translations with tracked changes
- Enterprise-grade security
End-to-end encryption and automatic file deletion
- Fast, scalable processing
Large files and batches processed within minutes
- Format-perfect translation
Original layout, styling, and structure maintained
How it works
Our streamlined process delivers fast, accurate, and format-perfect document translations.
Upload Your Files
Securely upload your documents (PDF, Word, Excel, images, etc.) to our platform.
Select Languages & Settings
Choose your target languages and any specific translation or formatting preferences.
Receive Instant Translation
Our AI engine processes your documents, preserving layout and delivering high-quality translations in minutes.
Review & Download
Download your translated documents, ready for immediate use, with original and translated content side-by-side.
Frequently Asked Questions
Get answers to common questions about our online document translation service. Learn about supported formats, security, turnaround time, and how to get started with instant translations.
Bluente's layout-aware translation engine preserves tables, charts, footnotes, numbered lists, and styles exactly as they appear in your original clinical trial documents. Our technology specifically handles complex structures common in consent forms, protocols, and regulatory submissions, ensuring that formatting integrity is maintained across all file types including PDF, DOCX, PPTX, and XLSX.
Yes, Bluente features advanced OCR (Optical Character Recognition) technology specifically designed for scanned clinical trial documentation. Our system converts non-selectable text in scanned PDFs and images into editable, searchable, and translatable content while maintaining the original layout, making it ideal for legacy documents and signed consent forms that exist only as scans.
Bluente provides enterprise-grade security for all clinical trial documentation. Your confidential patient data and proprietary research information are protected with encryption during processing, and all files are automatically deleted after translation. This approach ensures compliance with data protection regulations while maintaining the confidentiality requirements essential for clinical trials.
Bluente translates large clinical trial protocols and multi-document batches within minutes rather than days. Our platform is designed to handle high-volume, complex documents with speed and accuracy, enabling time-sensitive clinical trial workflows without sacrificing quality or formatting integrity.
Bluente supports translation of clinical trial documentation across 120+ languages, facilitating global clinical trials and regulatory submissions in multiple regions. All translations maintain the exact formatting and structure required for regulatory compliance, regardless of language pair.
Yes, Bluente generates side-by-side bilingual outputs that show original and translated content together. This is particularly valuable for consent forms where regulators often require both language versions for verification. These bilingual documents facilitate quick comparative review and ensure translation accuracy for patient-facing materials.
Bluente's AI-powered translation engine is built to handle specialized terminology with high accuracy. For clinical trial documentation, our system preserves complex medical terms, drug names, procedural descriptions, and technical language while maintaining contextual accuracy across all translated materials.
Translate Your Clinical Trial Documents Now
Secure, format-perfect translation ready for regulatory submission. Preserve layouts and data integrity while cutting translation time from days to minutes.
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