Tridion for medical devices
Create documentation that is accurate, consistent and compliant
Whether you’re creating an IFU or reporting to a regulator, you need to provide accurate, clear and consistent information.
A structured content approach makes this simple – by organizing all your technical information centrally, using predefined modules and relationships.
It allows medical device companies to create, manage and distribute multilingual technical documentation at scale, much more safely and efficiently, in compliance with regulations such as EU MDR and IVDR, while being prepared for future changes, including new regulations and data-driven submissions.