High-precision B2B translation and localization of regulatory dossiers, clinical trial protocols, and healthcare documentation. BuroPerevodov provides elite linguistic validation in compliance with global medical data security and strict NDA standards.
| ISO 17100 | ISO 9001:2015 | ISO 13485:2016 | 39+ Languages | Linguistic QA (LQA) |
Translation of Clinical Trial Protocols (CTPs), Investigator Brochures (IBs), Informed Consent Forms (ICFs), and complex pharmacology regulatory dossiers.
Localization of technical manuals, software interfaces, and Instructions for Use (IFU) for MRI systems, ventilators, and surgical hardware complexes.
Expert processing of validation reports, chemical patents, laboratory asset guides, and manufacturing batch records under EMA and FDA frameworks.
Includes full Translation Memory deployment and glossary validation
Multi-stage linguistic QA with final review executed by practicing MDs