Your technical documentation stays current while you focus on your devices. When standards shift, literature evolves, or guidance changes — Virgil catches it first.
How it works →Some companies need their MDR documentation written from scratch. Others already have a technical file that's falling behind. Either way, the problem is the same: regulatory requirements never stop changing, and traditional consultancies aren't built for ongoing work.
Virgil is built for both. Whether we create your documentation, update what you have, or maintain it going forward — a dedicated monitoring system watches the regulatory landscape on your behalf and tells you exactly what has changed, what it means for your devices, and what needs attention.
Every update to your technical file is reviewed and approved by an experienced regulatory professional before anything changes. No exceptions.
The technology watches everything. The human decides what matters.
Based in Berlin. Working with select medtech companies on MDR transition and ongoing documentation maintenance.
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