Is this a certified medical translation?
No. The downloadable PDF is an unreviewed machine-translation draft. Certified, sworn, notarized, or authority-ready translations require the appropriate qualified human translator and market-specific review.

Choose the regulatory document you need to translate. Every tool returns a free, layout-preserving five-page PDF draft, with task-specific guidance for IFUs, labels, technical dossiers, FDA documents, and submissions.
Start on the page that matches your document. The translator is shared, while the preparation, review checks, official sources, and next step are specific to the regulatory job.
Translate medical device instructions for use while retaining the PDF layout.
Open free toolTranslate medical device label copy, warnings, storage text, and packaging information.
Open free toolTranslate a technical dossier, technical file, test report, or evidence excerpt.
Open free toolTranslate forms, submission narratives, declarations, and authority correspondence.
Open free toolCreate an English draft of a foreign-language FDA source document or translate an FDA PDF.
Open free toolUse the general translator when one PDF combines labeling, technical evidence, forms, or correspondence. The same five-page and temporary-processing limits apply.
Medical device translation is determined by the target market, document type, intended user, and submission purpose. EU Member States set language requirements for information supplied with devices; Canada applies English and French labeling rules in defined circumstances; FDA expects English or an accurate English translation for specified submission material.
Use the free PDF as a scoping draft. Before release or submission, verify missing or added text, terminology consistency, warnings, numbers, units, product names, model and UDI identifiers, tables, OCR uncertainty, and whether the market requires a certified, sworn, or locally reviewed translation.


Need help confirming a classification or planning your registration?
Move the translated excerpt into a content review, market plan, or expert handoff with the document context still in mind.
Paste translated labeling evidence and screen intended use, warnings, directions, UDI, symbols, and claims.
Connect the product to country pathways, government fees, dossier preparation, review timelines, and next steps.
Test a current update against one product and create an owner-ready action workpaper.
No. The downloadable PDF is an unreviewed machine-translation draft. Certified, sworn, notarized, or authority-ready translations require the appropriate qualified human translator and market-specific review.
The tool translates pages 1 through 5. If the source PDF is shorter, it translates the whole file. Longer PDFs are physically trimmed before they are sent to Microsoft, so pages after page 5 are not processed.
Microsoft Document Translation is designed to preserve document structure and presentation. Complex scans, handwritten content, layered graphics, unusual fonts, tables, and text embedded in images can still require manual correction.
You can use the free output as a draft or scoping preview. Before submission, confirm the target-market language requirement, terminology, numbers, identifiers, warnings, tables, and any certified-translation requirement with a qualified reviewer.
The public five-page preview currently accepts PDF because PDF pages can be limited exactly and returned with stable pagination. Convert the excerpt you want reviewed to PDF. Pure Global can coordinate complete Word, PowerPoint, Excel, scanned, and multi-file translation projects.
The preview uses temporary processing storage and deletes source and translated files after the response. Do not upload patient-identifiable, export-controlled, or confidential information to a free public tool.