German Medical Translation Services

Yes. Our German medical translators have direct experience with BfArM submission formats and the specific terminology conventions used in German regulatory documentation.

Yes. We translate technical files, Instructions for Use (IFU), and clinical evidence summaries to meet EU MDR requirements for devices sold in Germany and other EU markets.

We build a project-specific glossary at the start and apply it consistently using CAT tools and translation memories throughout the entire dossier.

Yes. All translators and project managers sign GDPR-aligned data processing agreements before receiving any patient-identifiable or trial-confidential material. Files are transferred over encrypted channels, processed on secure infrastructure, and purged from our systems on project closure unless you request translation memory retention. DSGVO compliance (the German implementation of GDPR) is embedded in our standard clinical project workflow.

A standard informed consent form of 2,000 to 4,000 words delivers in 2 to 3 business days including QA. A full clinical study report or 50-page investigator brochure typically runs 5 to 10 business days depending on volume and annex count. For multi-language EU submissions we run German in parallel with French, Spanish, Italian, and Dutch under a single project manager to keep timelines tight across all language versions.