We translate clinical trial documentation for Clinical Research Organizations across more than 100 language groups
– quickly, accurately, and with an expertise based on over 40 years of producing IRB-compliant translations.
The Challenges We Address
We specialize in complex, multi-language Patient Consent packages.
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Dedicated and experienced project management.
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Time assurance – ready when we promise.
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Done right the first time.
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Formatted and ready to go.
How We Work
Every Clinical Trial project is assigned a dedicated project manager with many years of experience in clinical trials.
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Every project is given a clear and accurate target completion date.
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Clients can communicate with their Project Manager on the status of their project at any time.
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We use the leading translation portal technology.
Why Work With DTS?
Our global teams specialize in Clinical Trial Translations.
- Our project teams understand the timing, accuracy and budget realities of these projects.
- We’ve translated over five thousand clinical trial-related document packages for over fifty life science companies in the last 2 years alone.
“DTS did an excellent job with translations for Alveolus (medical device company). I would highly recommend DTS Language Services to any pharma/medical device colleagues. DTS did a cost-effective, punctual, and excellent job translating as well as providing translation certificates. ”
Rita Lee – Senior Manager Regulatory Affairs at United Therapeutics Corporation
Need Help? Let’s Discuss Your Next Project!
Top 10 Criteria for Selecting a Translation Specialist for your Clinical Trial Documents
- Verify target language proficiency.
- Confirm “all in” project pricing (“per word” charges are just part of the total cost on most projects – are there other fees or costs?)
- Validate timing promises:
>> Time to get a quote?
>> Translation delivery timeline?
>> Rush options, if any? - Ask if your actual translators have “subject matter” understanding and experience.
- Confirm that all the work will be Certified.
- Confirm that all the work is IRB compliant.
- Ask how they manage “site specific” consistency and costs across a study.
- Confirm that you will work with a dedicated Project Manager.
- Ask if English “back translations” are available or standard.
- Ask if the company is ISO certified.
Need Help? Let’s Discuss Your Next Project!
Clinical Trial Translations is what we do.
We deliver a headache-free experience of certified translations, guaranteed turn-around time, and responsive project management.


