Go global faster with our language and content solutions

DIA Europe | March 12-14, 2024 | Brussels, Belgium

Thank you to everyone who visited us at DIA Europe 2024

RWS is a leading provider of language and structured content authoring solutions – working with 19 of the world's top 20 pharma companies.

We can help you with clinical trial management, linguistic validation, labelling and much more in any language.

Discover who we are

Tridion Docs for medical devices

Specialized towards Medical Device IFUs and Regulatory Submissions, Tridion Docs takes the pain out of managing your documentation and MDR / IVDR requirements, while working with your existing RIM systems.

Fonto Integrated Authoring Platform

Developed in collaboration with leading pharma companies – Fonto IAP combines the power of structured content with user-friendly, data-driven authoring, using AI tools in the best possible ways.

RWS Life Sciences

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

Blogs from RWS

Enhancing Veeva Vault’s content management capabilities with Tridion Docs

Recently, Tridion’s team convened with its partner Prana Life Sciences LLC (PLS), to discuss the joint value proposition of both companies. Read this blog for an overview of this discussion.

Read blog

Embracing the future of document authoring in pharma: a structured and data-driven approach

In the fast-paced world of pharmaceuticals, the clarity and precision of documentation are not just a matter of compliance, but a cornerstone of innovation and patient safety. Read this blog to discover more.

Read blog

Digitization. The way forward for regulatory labelling

In this blog, we shed a light on the regulatory challenges the global pharmaceutical industry faces, focusing on the European Medicines Agency (EMA) as a prime example.

Read blog