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.
Intelligent content for medical technical files
Use componentized content to create accurate, organized files for submission – and keep track of your edits every step of the way. With our structured content authoring tools, you can write, review, approve, translate, and maintain up-to-date documentation.
Create consistent, high-quality, on-time regulatory submissions with Tridion Docs
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Five reasons to use structured content for your regulatory submissions
Increase product safety and traceability from design concept to post-market activities
Streamlined connected collaboration
Compatible with your eQMS
Content and translation reuse
100% reliable audit trail
Omnichannel publishing
Discover how our clients write and publish content faster with Tridion Docs
Want to explore how to optimize your regulatory submission processes?
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