Free regulatory document translation

Free regulatory submission translation

Translate the first five pages of a medical device submission, application, declaration, or authority document. Download a working PDF draft for local regulatory and linguistic review.

First 5 pages free39 target languagesDirect PDF downloadNo account required

Translate a regulatory submission PDF

First 5 pages · no signup

Translate to

More languages

Temporary files are deleted after processing. Do not upload patient-identifiable or confidential information. Output is an unreviewed machine-translation draft.

Use the same tool for this exact task

Use the preview across a regulatory submission workflow

Submission translation connects product facts, controlled terminology, forms, evidence, and authority questions. A bounded preview helps the project team establish the translation approach before processing the full application package.

Application forms, cover letters, declarations, certificates, and authority correspondence.

Device descriptions, intended purpose, classification statements, manufacturing summaries, and route rationales.

Responses to questions, deficiency letters, change notifications, and lifecycle submissions.

Local documents that need an English working draft for a global regulatory team.

DJ Fang

MedTech Regulatory Expert

Need help confirming a classification or planning your registration?

Pricing

Review before use

Submission translation review points

The translation should agree with the source file and the rest of the application—not introduce a new product position.

Reconcile names, addresses, roles, registration numbers, models, dates, and declarations across the package.

Keep classification, intended-purpose, manufacturing, and evidence terminology consistent with controlled documents.

Confirm signatures, stamps, attachments, tables, form fields, and authority question numbering are accounted for.

Determine whether the authority requires an accurate, certified, sworn, notarized, or locally reviewed translation.

Regulatory boundary

Free translation does not determine submission acceptability

Authorities and markets apply different language and certification requirements. Treat the preview as a working draft, then have the complete document set reconciled and reviewed for the specific submission.

Medical device translation hub

Translate another regulatory document

Each page uses the same free translation engine, but gives you the review context for a different medical-device document and search task.

IFU translation

Translate medical device instructions for use while retaining the PDF layout.

Label translation

Translate medical device label copy, warnings, storage text, and packaging information.

Technical dossier translation

Translate a technical dossier, technical file, test report, or evidence excerpt.

FDA document translation

Create an English draft of a foreign-language FDA source document or translate an FDA PDF.

View all translation tools

About this tool

Regulatory submission translation: what to know before relying on the draft

The translator returns an unreviewed machine-translation draft of the first five pages. Use it for scoping and internal review; confirm terminology, identifiers, warnings, and any certified-translation requirement before release or submission.

Can I translate a regulatory submission for free?: You can translate the first five pages of a PDF into one target language for free. The result is a draft and is not an authority-approved or certified translation.
Which regulatory documents can I test?: Typical excerpts include application forms, declarations, cover letters, certificates, authority questions, response letters, and device-description sections.
Will the tool certify or notarize the translation?: No. Certification, sworn translation, notarization, and in-country review require qualified people and processes outside this free preview.