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.

Serving 19 of the top 20 pharmaceutical companies

Helping 9 of the top 10 medical device companies

Working with 10 of the top 10 Contract Research Organizations.

1,750+ in-house linguistic experts globally

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.

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Linguistic Validation

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

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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.

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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.

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Solutions

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.

Translate global clinical trial documents

Establish a scalable translation model that can adhere to the milestone requirements, from clinical trial study start-ups, to regulatory submissions. We can help facilitate through all phases of your clinical trial, covering file preparation, translation and review, desktop publishing, and quality assurance.

Our model incorporates a follow-the-sun methodology and leverages resources in multiple regions around the world.

Secure the translation supply chain

Increase the efficiency of projects with technology enabled translations choosing from a full range of deployment options to streamline your localization projects.

Our technology is secure by design and our quality processes are based on our deep understanding of the regulations involved—including FDA, MHRA, and MHLW—so you can have peace of mind for all of your regulated content.

Manage regulatory compliance document demands

If you are still using traditional methods of documentation, delivering high-quality, timely publications can be challenging.

Adopt a centralized knowledge hub to align teams, create robust translation, and review processes—including oversight and audit tracking—drive content reuse, and promote standardization so you can speed up content changes.

“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.

“SDL helped us understand the paradigm shift required to move to this new environment. We particularly appreciated that SDL was committed to helping us configure the system to meet our needs rather than forcing us to adopt a particular, predefined method of use.”

Joshua Steen, Principal Technical Writer and Tools Specialist.

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