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Medical translation by domain-qualified linguists

Healthcare Localization & Medical Translation

Pubrica provides medical translation and healthcare localization for pharma and medtech companies launching in new markets, clinical trial sponsors, hospital systems, medical device manufacturers and patient advocacy organizations. Each project delivers the translated document in the target language, a linguistic and subject-matter-expert review confirmation, a terminology glossary for the language pair, a print- or web-ready formatted file and, where required, a back-translation report, with quality assurance aligned to ISO 17100. Translation is carried out in-house by domain-qualified linguists. A named subject specialist manages your project from brief to delivery, and a second, independent reviewer checks the translation before it reaches you.

  • Translated document in target language — included in every engagement
  • Linguistic/subject-matter-expert review confirmation — included in every engagement
  • Optional back-translation report — included in every engagement
  • Produced to named standards, including ISO 17100
  • A published starting price: $0.22/word for the standard scope
What is included What is not included

Translated document in target languageIncluded

Linguistic/subject-matter-expert review confirmationIncluded

Optional back-translation reportIncluded

Terminology glossary for the language pairIncluded

Work outside the agreed scopeNot included

Brief → scoping → draft → delivered

Every engagement
  • Translated document in target language
  • Linguistic/subject-matter-expert review confirmation
  • Optional back-translation report
  • Terminology glossary for the language pair
  • Print- or web-ready formatted file
$0.22/wordPublished starting price
5–10 business daysFrom brief to final delivery
5 deliverablesListed in full below
ISO 9001:2015Quality management certified · cert. H3CR9TCU20251212INDQM10N

Deliverables

Five Deliverables in Every Medical Translation Project

Every item below is produced in-house by Pubrica’s domain-qualified linguists and checked by a second, independent reviewer before delivery.

Translated document in target language Translated document in target language.
Linguistic/subject-matter-expert review confirmation Linguistic/subject-matter-expert review confirmation.
Optional back-translation report Optional back-translation report.
Terminology glossary for the language pair Terminology glossary for the language pair.
Print- or web-ready formatted file Print- or web-ready formatted file.

Who We Serve

Five Client Groups We Support with Medical Translation and Healthcare Localization

The organizations below commission this service, and each project is planned around the audience who will use the material.

Pharma and medtech companies launching in new marketsA client group that commissions this service directly.
Clinical trial sponsors translating patient-facing consent and instruction materialsA client group that commissions this service directly.
Hospital systems serving multilingual patient populationsA client group that commissions this service directly.
Medical device manufacturers with labeling/IFU translation needsA client group that commissions this service directly.
Patient advocacy organizations localizing educational materialsA client group that commissions this service directly.

Compliance and Standards

Four Standards and Guidelines Applied to Medical Translation and Healthcare Localization

The regulatory codes, guidelines and quality standards that apply to this service.

ISO

ISO 17100

ISO 17100 is the recognized quality standard for translation service provision and is commonly cited by medical translation providers.

ISO

ISO 13485

ISO 13485 applies when translated content relates to medical devices, because device documentation falls under device quality-management requirements.

FDAEMA

FDA / EMA regulatory guidelines

FDA and EMA guidelines govern the regulatory and labeling content being translated, independently of the translation process itself.

ISO9001:2015

Quality management (cert. H3CR9TCU20251212INDQM10N)

Governs how each project is managed, reviewed and documented.

Responsible Use of AI

Our Approach to AI Use in Medical Translation and Healthcare Localization

Generative tools are useful for drafting and iteration. They are not used anywhere the output could be mistaken for verified clinical data or a real patient.

What we use it forLayout variations, colour systems, and first-pass drafts that a human then corrects against the brief and the brand or clinical standards that apply.
What we do not use it forGenerating any image, figure or quote presented as real clinical data, a real patient, or a verified result; and nothing goes out without a named reviewer's sign-off.
What we include in your AI declarationThe tool, the stage it was used at, and the human oversight applied — because MLR/PRC reviewers, funders and regulators increasingly expect this stated rather than assumed.

Why we do not publish AI accuracy figures

Accuracy figures for AI design and content tools are usually reported by the vendors that sell them.

For this reason we do not quote an accuracy figure of our own. We tell you which tool was used on your project, at which stage, and what a named reviewer changed afterwards.

Our Process

How Our Medical Translation Process Works

Each project moves from brief and scoping to a reviewed first draft, then to revisions and final delivery.

Step one

Submit Your Brief and Reference Material

Send us the source material, details of who the translation is for and anything that must or must not appear, together with any existing assets, brand guidelines or reference material we should work from.

Step two

Scoping Consultation

We confirm the audience, the applicable standards and, for scoped work, the factors that determine the final price, so the quote is agreed before work begins.

Step three

Concept and First Draft

A subject specialist and the production team build the first version against the brief, reviewed internally for accuracy before it reaches you.

Step four

Revisions and Final Delivery

We incorporate your revisions and deliver the files listed on this page, including the working files, so the material can be updated later without starting again.

Request a Free Scoping Assessment for Your Medical Translation Project

We confirm the cost, timeline and applicable standards before you commit to anything. The assessment is free and is completed within two business days.

What you provide
The briefThe purpose of the material and its intended audience
Reference materialExisting assets, brand or style guidelines, prior approved versions
The audienceClinician, patient, payer, investor or internal team
ConstraintsAnything that must or must not appear, and the standards that apply
The deadlineYour deadline, including any congress or submission window
Approval routeWho approves the work, and whether MLR/PRC review is part of the process

Our Experts

Your Medical Translation Team

The same named team of specialists stays with your project from scoping to delivery.

Subject expertSubject matter expert matched to your topic

Determines which claims the evidence supports. The subject expert is matched to your topic and tells you clearly when the brief asks for something the evidence does not support.

OwnsScope, judgement, interpretation
Reviews againstThe applicable standards for this work
FieldMatched to your topic
Dr. DivyaPhD in Life Science · second reviewer

Reviews the work independently of the first pass and reconciles the two, because most errors in this work are factual rather than errors of reasoning. Disagreements are logged and adjudicated.

OwnsIndependent second read
Reviews againstThe applicable checklist
Adjudicated byA third reviewer
Dr. AntonyProduction and delivery lead

Responsible for file formats, compliance with the destination specification and the handover of working files, so that the delivered files match what you requested.

OwnsProduction and delivery
Reviews againstThe destination's own specification
Second-checked byA second production reviewer
Mr. JohnCompliance and standards reviewer

Confirms that the work meets the standards that apply to it, whether MLR, WCAG, a regulatory guidance or the body that governs the specific deliverable.

OwnsStandards and compliance review
Reviews againstThe standards listed on this page
ToolsThe current published guidance for each

Evidence Base

Evidence Informing Our Medical Translation Approach

Each point below is sourced from published research or guidance, or owned by a named role on the team. We can direct you to the source or the reviewer on request.

01 Medical translation vendors structure pricing around three models -- per-word,...Medical translation vendors structure pricing around three models -- per-word, per-page, and project-based -- with cost driven by domain expertise, language pair, and depth of quality assurance rather than a single flat industry rate.
02 Recognized ISO standards for medical translationMedical translation providers commonly cite ISO 17100 (translation services) and ISO 9001 (quality management), plus ISO 13485 when working on medical device content, alongside the FDA and EMA requirements that govern the underlying material.
03 Back-translation -- having a second, independent translator render the translated text...Back-translation -- having a second, independent translator render the translated text back into the source language to catch discrepancies -- is presented by vendors as an advanced, optional validation step, alongside linguistic validation by native speakers and subject-matter experts, rather than a universal default.
04 Professional translation for patient materialsPlain-language health communication guidance recommends professional translation, or translation developed together with community members, rather than relying on direct/literal translation alone when localizing patient materials.

Packages

Medical Translation Pricing: Published Starting Price

The published starting price below covers the standard scope; larger projects are quoted before work begins.

Standard

Healthcare Localization & Medical Translation

Fixed price per source word, per target language, for standard medical/patient-facing content translation including one subject-matter-expert linguistic review pass; back-translation and additional validation rounds are quoted as add-ons per language.

$0.22/wordPublished starting price

Delivery 5–10 business days

  • ✓Translated document in target language
  • ✓Linguistic/subject-matter-expert review confirmation
  • ✓Optional back-translation report
  • ✓Terminology glossary for the language pair
  • ✓Print- or web-ready formatted file
Get a free quote

Quality Assurance

Our Service Commitment

The revision commitment that applies to every project, with its scope and remedy stated in advance.

The Pubrica revision commitment

Free Revision When Work Does Not Meet the Agreed Brief or Named Standard

Within the agreed scope, we revise at no extra cost any work that does not match the brief or a standard named on this page.

01

The brief is confirmed before production

Confirming the brief at scoping prevents misunderstandings that would otherwise require rework after delivery.

02

A named reviewer signs off before you see it

The review is made against the standards listed on this page.

03

AI use is disclosed

We tell you which tool was used, at which stage, and what a human reviewer changed afterwards.

04

You receive the working files

The material can be updated later without starting again or paying for the work twice.

Client Stories

“The content cleared MLR on the first pass, which almost never happens with an outside writer.”
HarrisMedical affairs lead, pharmaceutical company

FAQs

Frequently Asked Questions About Medical Translation and Healthcare Localization

If your question is not answered here, ask an expert — no quote required.

Pubrica provides medical translation and healthcare localization for pharma and medtech companies launching in new markets, clinical trial sponsors, hospital systems, medical device manufacturers and patient advocacy organizations. Each project delivers the translated document in the target language, a linguistic and subject-matter-expert review confirmation, a terminology glossary for the language pair, a print- or web-ready formatted file and, where required, a back-translation report, with quality assurance aligned to ISO 17100. Translation is carried out in-house by domain-qualified linguists. A named subject specialist manages your project from brief to delivery, and a second, independent reviewer checks the translation before it reaches you.

The core deliverable is the translated document in the target language; the full list appears under “Deliverables” on this page.

Medical translation vendors structure pricing around three models -- per-word, per-page, and project-based -- with cost driven by domain expertise, language pair, and depth of quality assurance rather than a single flat industry rate.

This requirement is documented in published research and regulatory guidance, so our specialists address it as a defined part of every project.

The published starting price is $0.22/word, charged per source word and per target language, for standard medical and patient-facing content, including one subject-matter-expert linguistic review pass. Back-translation and additional validation rounds are quoted as add-ons per language, and any work beyond the standard scope is quoted before it begins.

Pharma and medtech companies launching in new markets

Clinical trial sponsors translating patient-facing consent and instruction materials

ISO 17100 is the recognized quality standard for translation service provision and is commonly cited by medical translation providers.

We apply this standard from the start of each project rather than correcting for it after a reviewer raises it.

Request a Free Scoping Assessment for Your Medical Translation Project

Receive a free assessment of cost, timeline and applicable standards within two business days.

Get a free quote

Regulations

Check your project against this rule

  1. 1Your work
  2. 2Your details
  3. 3Send
What do you need?

Material you send is held under signed confidentiality, with access limited to the assigned team and encrypted transfer. It is not used to train anything and is not passed to third-party tools. Ask for the agreement before you send anything you would rather cover first.