We translate clinical trial documentation for Clinical Research Organizations across more than 100 language groups
– quickly, accurately, and with an expertise based on almost 50 years of producing IRB-compliant translations.
The Challenges We Address
We specialize in complex, multi-language Patient Consent packages.
- Projects that require dedicated and experienced project management.
- Projects that need timely delivery – available when promised on a consistent basis.
- Projects that need to be done right the first time – without a lot of back and forth.
- Projects that are expertly formatted and ready to go when delivered.
Click here for a list of some of the common document types we translate.
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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 type of projects.
- We’ve translated over five thousand clinical trial-related document packages for over fifty life science companies in the last 2 years alone.
“I have had the experience of working with the DTS Team for translation needs over a span of 16 years. DTS always provided top quality and 100% accuracy on all translated documents. The DTS Team is always professional and go to great lengths to meet all timelines.
I highly recommend DTS for all your translation needs.”
Therese Allen, WCG IRB See more testimonials
