Create compliant regulatory submissions for medical devices and IVDs
Efficient. Accurate. Traceable.
Collate technical documentation at warp speed with cloud-based structured content authoring. By taking a content-centric approach to your submissions, you can collaborate seamlessly between internal stakeholders and external regulatory agencies to produce complete, compliant and up-to-date documentation.
Structured content is the foundation for centralized, automated regulatory submission processes. It breaks your content down into reusable components, so your teams can create multiple documents at the same time using the latest approved technical information – and update them just as easily.