IVDR solution brief

In vitro diagnostic device companies are facing new challenges in creating, managing, translating, submitting and delivering content and technical documentation in accordance with all the In Vitro Diagnostic Medical Device Regulation (IVDR) requirements – including additional documentation that must be presented and translated in all 24 EU languages much earlier in the certification process.

We offer a range of content solutions to guide you through the complexities of IVDR compliance and the creation of any audit-ready multilingual technical documentation that you are required to produce.

Download our solution brief to learn more about how we can help you ensure IVDR compliance – now and in the future.