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Resources

What we have learned, made usable.

We turn what we learn from the health tech ecosystem into practical tools,
insights and resources that companies can actually use.

Regulatory support

The regulatory jungle,
mapped.

Regulatory approval is one of the greatest barriers for the companies we work with. Approval takes around twice as long in Europe under MDR as it does in the US — so companies launch there first, and some never launch here at all.

To strengthen health tech in Denmark and Europe, we built Health Tech Pathways with support from the Novo Nordisk Foundation. It is an AI-guided platform for health tech companies building medical device software. Describe what you are making, and it works out whether MDR applies, which risk class you fall into, and the route from there.

Members get a 50% discount on the full platform.

What our members say.

“Before Health Tech Pathways, regulatory compliance felt like a black box. The platform breaks the process down into manageable steps and helps us understand exactly what needs to be done.”

— Mads Skak, CTO · Cacto Health

“It’s great to see how Health Tech Pathways can make one of the hardest parts of health tech innovation — regulatory approval — more accessible for early-stage hospital projects.”

— Rasmus Fält, Accelerator Lead · BETA.HEALTH

Explore Health Tech Pathways

Reports

What we found out
when we went looking.

Research and perspectives from our work across the ecosystem. We do not publish often — only when we could not find the answer anywhere else and had to go and ask.