What is a technical document translator?
It translates specialized content while keeping technical terms, identifiers, numbers, tables, and document structure usable for subject-matter review. This free version returns a five-page PDF draft.

Upload an excerpt from a technical dossier, technical file, test report, risk document, or clinical evidence PDF. Translate the first five pages and preserve the page layout for subject-matter review.
A dossier translation has to preserve traceability across sections, evidence, tables, references, and controlled terminology. Use the preview to identify terminology and layout issues before translating the complete package.


Need help confirming a classification or planning your registration?
Reviewers should be able to trace a translated statement back to the same evidence and requirement in the source file.
The free tool processes only the first five PDF pages and does not validate the technical evidence, reconcile the full submission, or certify the translation. Use it to scope the work and establish terminology before full document control and review.
Each page uses the same free translation engine, but gives you the review context for a different medical-device document and search task.
Translate medical device instructions for use while retaining the PDF layout.
Translate medical device label copy, warnings, storage text, and packaging information.
Translate forms, submission narratives, declarations, and authority correspondence.
Create an English draft of a foreign-language FDA source document or translate an FDA PDF.
It translates specialized content while keeping technical terms, identifiers, numbers, tables, and document structure usable for subject-matter review. This free version returns a five-page PDF draft.
Yes, you can translate the first five PDF pages at no cost. Use a representative excerpt to test terminology and formatting before planning the full dossier.
No. The tool translates the PDF excerpt; it does not determine whether the dossier is complete, technically correct, or sufficient for a specific authority.
Do not place confidential, export-controlled, patient-identifiable, or commercially sensitive material in a free public tool. Use a suitable secure project channel for complete dossiers.