SDL Life Sciences

Life Sciences

Gain greater process efficiency, reduce translation costs, and speed up go-to-market with our specialized language, COA and content solutions across life sciences, medical research, and contract research organizations (CROs). 

Now you can create real value for your teams and ecosystem partners to drive better outcomes for scientists, medical representatives, professionals, and patients alike.

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Why RWS?

Address scalability, accuracy, quality, and compliance across the value chain with an organization you can trust.
Test tubes

Serving 19 of the 20 top pharmaceutical companies.
Medical Device

Helping 19 of the 20 top medical device companies.
Certification

Working with 8 of the top 10 Contract Research Organizations.
Person access

1,400+ in-house linguists.
Calendar

24/7/365 support across the globe.

Areas of expertise

Comprehensive content and language solutions for the Life Sciences industry.

Clinical Trial Management

When clients need translations for clinical trial documentation, they can rely on RWS – the leading and trusted authority in clinical trial translation services – to get it done right the first time, every time.

Linguistic Validation

RWS is the preferred and trusted authority for linguistic validation and management of Clinical Outcomes Assessments (COA).

Regulatory Affairs/Submissions

Translating product materials accurately is our number one priority. Our industry specialization, regulatory knowledge and terminology expertise ensures it is always done correctly and on time.

Medical and In-Vitro Device Services

In addition to our exclusive focus on the life sciences industry, we have a team of highly specialized translation experts and linguists who are dedicated to managing the unique nuances of medical device projects.

Solutions

Document charts outward arrows

Manage multilingual regulatory labelling & submissions

Streamline complex labeling requirements and maintain accurate product information globally. 

Our solution enables you to capture and track label changes, reuse regulated-approved translations, simplify review process, as well as lower the cost of translation workload.

Manage multilingual regulatory labelling & submissions
Translate global clinical trial documents
Secure the translation supply chain
Manage regulatory compliance document demands
Agfa Healthcare
“Previously, the average overall quality of first-time translation was 75%. Today, using MultiTerm, we are achieving 95% rate of quality in the translations. That cascades down into enhanced brand recognition, and improved productivity.”

Hans Fiers, Documentation and Localization Manager for Radiology and Clinical Information Systems.