We are Escentia
What we believe in
We believe that behind every medical device is a story: a grandmother who wants to garden again, a parent who wants to see their child graduate, a partner who wants more mornings together. Their health isn’t just their own; it’s woven into the lives of everyone who loves them. That’s why we do this work: to make sure regulations serve those stories instead of stalling them, so treatment arrives when it matters most.
How we bring it to life
We approach regulation as a scientific and strategic problem, not a box-ticking exercise. We translate complex regulatory and clinical requirements into clear evidence strategies. We partner with companies to prove safety and efficacy without unnecessary delays. We challenge the status quo and focus on what can be shown convincingly, not on what is done by habit.
What We Do
We help medical device companies design and execute evidence strategies with confidence. If you join us you’ll spend your days solving the translation problem that sits at the heart of medtech and help companies turning technical performance, risk controls, and non-clinical data into coherent clinical evidence that regulators understand and trust.
You’ll work directly with clients‘ regulatory and product teams, delivering documented evidence that moves projects forward instead of creating busywork.
Our culture
Open Jobs
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