Pharmaceuticals translation services built for regulatory compliance
Pharma teams need regulatory dossiers, patient materials, staff training, and promotional content rendered exactly across languages. ABC Translations handles pharmaceutical translation in 120+ languages at $0.09 per word on average, delivered fast with unlimited revisions.

An error in a filing can delay an approval by months
Pharma runs on documents that agencies read word by word. A clinical trial protocol, a regulatory filing, a patient information leaflet, a product label. One mistranslation can delay an approval, create a patient safety risk, or trigger a significant financial penalty.
Few industries face the scrutiny yours does, and reaching a market hinges on language that is correct from the very first submission. Approximate is not a category that exists here.
Your timeline and your patients stay protected by certified translation that meets what regulators such as the FDA and EMA demand, done by linguists fluent in the language of compliance.
Certified and professional translations for the pharmaceutical industry
Promotional campaigns, staff training, and materials that educate patients run as professional translation, priced at $0.09 per word, with every job assigned to native-speaking professionals working across 120+ languages.
At $24.10 per page, ABC Translations certifies the documents regulators study most closely, including drug approval submissions, study protocols, and labeling that bodies such as the FDA and EMA require.
Certified regulatory filings arrive within 48 hours; standard per-word work is delivered on a timeline set by the project's size. Every order comes with as many revisions as you need, and a rush option is available whenever a deadline cannot wait. Support patient safety through accuracy and protect market access in every region you file in.


Pharmaceutical documents we translate
Day to day we work on study documentation for trials, submissions to regulators, leaflets that inform patients, and labels for products, along with paperwork for medical devices, patent submissions, and materials proving regulatory compliance. The translators on this work understand both the science and the regulatory expectations.
Why pharmaceutical companies choose ABC Translations
Over 25 years, more than 255,000 customers have relied on ABC Translations to keep clinical, regulatory, and labeling documents precise, compliant, and ready for the agencies that decide whether a drug can reach patients.
Send us your regulatory and clinical documents today and get certified translations back within 48 hours.

Pharmaceutical paperwork our linguists regularly handle
Drug companies bring us their device paperwork, submissions for patents, and compliance documentation, the files we translate most, each prepared to the exact precision regulators demand.
What makes ABC Translations the right fit for pharmaceutical paperwork?
Drug makers and research sponsors rely on us for accurate translations built around strict regulatory expectations. Trial protocols, labeling, and regulatory submissions are handled by professional native-speaking linguists who keep every term and dosage exact, treating each document with care and meeting demanding approval timelines.
Have more questions about pharmaceuticals translations? Find out more over in the help center:
ABC Translations help centerPrecise work from native speakers
- Native-speaking linguists handle every project, catching the subtle shades of meaning that keep your message accurate, clear, and true to its culture.
Quick, dependable, and protected
- You get fast turnaround without any drop in quality, backed by tight confidentiality and data security from start to finish.
Support that actually helps
- A responsive team stands ready at each step, so the whole process feels smooth, professional, and free of stress.
Our services
Either choice gives you polished, human-made work from professional linguists. Not sure if certification applies to your case? Ask whoever will receive the document, or reach out to our team.
How it works
Thanks to a simple, well-organized workflow, having your paperwork translated is fast and hassle-free.
Upload documents & place your order
Pick the two languages, send over your files, and choose any extras you want, then we get moving on your translation right away.
Professional translation and review
Your document is translated with care by a professional linguist. Before anything is locked in, you get to look it over and ask for changes.
Receive your translation
Once finished, the translated files are sent to you, and when you have chosen certification, a signed, stamped certificate on our letterhead comes with them.
Join 255,000+ happy customers
ABC Translations and its family of companies are proud to have delivered reliable, affordable, best-in-class translation and localization services to individuals, and global corporations and institutions for more than 25 years.
Join 255,000+ happy customers
ABC Translations and its family of companies are proud to have delivered reliable, affordable, best-in-class translation and localization services to individuals, and global corporations and institutions for more than 25 years.
Frequently Asked Questions
Find clear answers to the questions people most often ask about working with us. See how the workflow runs, what it costs, how long it takes, where documents are accepted, which notarization choices exist, and the way finished files reach you.
Are your certified translations prepared for FDA and EMA drug approval filings?
Yes. Submissions for drug approval, the protocols behind clinical trials, and labeling on products are rendered to the level regulators such as the FDA and EMA expect, and each carries a signed certificate confirming accuracy.
If an agency raises an issue with the translation during review, we revise it at no extra cost, so a wording problem does not stall your submission.
What does it cost to translate clinical trial protocols and patient information leaflets?
Patient education, training, and marketing materials average $0.09 per word as professional translation. Certified files, such as approval submissions, trial protocols, and product labels, run $24.10 per page.
Pricing is flat and shown before you order, so a full regulatory dossier can be budgeted with no surprises.
Can you handle pharmacovigilance and clinical terminology correctly?
Yes. Clinical trial documentation, pharmacovigilance reports, and product labeling are assigned to native-speaking translators with relevant scientific and regulatory backgrounds, so technical terms read correctly to both reviewers and patients.
Every order includes unlimited revisions, so any term can be aligned with your approved terminology before submission.
Can you keep product labeling and leaflet terminology consistent across markets?
Yes. For multi-market filings, we keep drug names, indications, and warning language consistent across every product label and patient information leaflet. Unlimited revisions let us match your master terminology so the same product reads the same way in each region.
Are confidential clinical trial and regulatory documents kept secure?
Yes. Clinical trial documentation, regulatory filings, and patent filings are handled under strict confidentiality, we can sign a non-disclosure agreement, and files move through secure transfer. Every translator on pharmaceutical work is bound by confidentiality requirements.
Which languages do you cover for global drug filings?
We translate pharmaceutical work across 120+ languages, so one provider can support your filings, labeling, and patient materials in every market where you seek approval.
















