Medical Device Regulation

Regulatory authorities under the EU MDR set strict demands for systematic literature reviews to ensure compliance and product safety. Meeting these requirements can be complex and time-consuming, but Silvi makes the process seamless by reducing manual workload, and focus on your core competencies: Delivering safe, reliable medical devices.

Always up-to-date

Let your review stay up to date with the latest research when new studies are published.

Fast reviews

Speed up your literature review process using the Silvi AI for screening and extraction.

Collaboration

Collaborate on your reviews to ensure high quality adhering to best practices for evidence generation.

Want to know more?

Do you want to know more about how you can use Silvi for MDR then let us contact you!