RWS provides translation, content management, and intellectual property capabilities for the medical device and in-vitro diagnostic (IVD) industries. We connect our clients with companies worldwide by communicating content at scale to help protect and realise ideas and innovations.
Our teams offer localisation, translation and transcreation services, as well as translation management technology, machine translation, and translation productivity tools, to help companies expand their global reach.
RWS’ solutions can improve the efficiency of translation processes and reduce their costs, as well as shorten times to market. By making use of our capabilities, you can create real value for your teams and ecosystem partners to improve translation outcomes for scientists, medical representatives and professionals, in addition to patients.
Accurate translations for the medical device industry
RWS can confidently handle all requests for translations through our understanding of and emphasis on the medical device and IVD industries.
We begin by thoroughly analysing projects to decide the most appropriate translation solution for each request and can adapt our methods to meet clients’ needs as necessary. We follow flexible procedures that allow us to deliver the most timely and cost-effective results.
Clear, compliant information for medical device products
The translation of information related to the production, distribution, and use of medical and IVD devices is essential for companies that serve global populations—and it presents several challenges. Translating information for medical and IVD companies requires not only linguistic skills but a deep understanding of the industry and highly specialised regulatory knowledge.
For more than 30 years, RWS Life Sciences has been a trusted partner to medical and IVD companies, offering ISO-certified multilingual solutions and translation services in more than 330 language variants. Our decades of dedicated partnerships have led to a deep understanding of the industries in which our clients operate.
Expert services for medical device and IVD companies
RWS’ global team of account managers, project managers, tested linguists, reviewers, terminologists, linguistic engineers, solution architects, and subject matter experts have deep translation, localisation, and regulatory experience.
We can deliver your translated multilingual content quickly, correctly, and in compliance with the Medical Device Regulation 2017/745 (MDR) and In Vitro Diagnostics regulation 2017/746 (IVDR) in all target markets.
We understand that our clients need to work with a partner that has extensive industry experience, can deliver a team of highly specialised translators who are both linguistic and subject matter experts, and can provide insights and validation regarding the regulations that govern the development and trade of medical devices worldwide.
In addition, RWS knows that high-quality, compliant content is critical for your work at every stage of the value chain, from research and development (R&D) to production to patient engagement. To complement our linguistic work, we offer a full suite of consulting, engineering, and business intelligence services.
