What counts as digital health here
Any company applying software, AI or connected devices to clinical care, diagnostics, monitoring or health-system operations – ambient clinical documentation, remote patient monitoring, diagnostics AI, longevity and ageing science, and hospital or care-coordination software. We include medtech-adjacent digital products and exclude pure biotech and drug discovery, which are filed under Biotech and pharma.
- Family
- Health
- Coverage since
- 2019
- Desks
- 4
- Reviewed
- 20 Sep 2026
The four desks
Each one is a live page – this pillar is the way in
Funding rounds
Every European digital health round we have verified with the company or the lead investor.
DirectoryStartup directory
Who is building what, at which stage, in which country – filtered to the vertical.
DirectoryInvestors
Funds and angels with a digital health thesis, ticket and stage – not a paid list.
RankingEvents
Trade shows, deal rooms and buyer fairs assessed for this vertical.
The 8 sub-verticals
Filter the startup desk by any of these
Where the companies are
Headquarters counted on the startup desk
Where the sector stands
Three eras, not a straight line
Pandemic-era demand pulled forward years of adoption for video consultation and remote triage. Much of it reversed once in-person care resumed.
Buyers stopped accepting a slick interface as proof of value. Companies without FDA clearance, CE marking or peer-reviewed outcomes data struggled to close hospital deals.
The largest rounds now go to ambient scribes and platforms aiming to become the clinic operating system, not point solutions – Tandem Health's raise is the clearest example.
Three open questions
Where informed people in this sector genuinely disagree
Every ambient-documentation vendor on this desk cites a time-saved statistic; almost none publish an independent audit.
CE marking and clinical validation take longer in Europe than the US regulatory path for comparable software.
Longevity has attracted serious capital, but most interventions being funded will not have outcome data for a decade or more.
How to get in
Three audiences, three short lists
If you are building
- Start the regulatory conversation with a notified body in your first six months, not your third year.
- Get one hospital or clinic to use your product in a real workflow before you pitch clinical impact – a pilot beats a deck every time.
- Decide early whether you are a point solution or a platform play; the funding available and the buyer conversation differ enormously.
- Pick two events: one clinical buyer show, one investor-facing deal room.
If you are investing
- Ask for the clinical evidence status explicitly – published, submitted, or aspirational – before you ask about the TAM slide.
- Underwrite the regulatory clock as a real cost, not a formality; it is the single biggest timeline risk in this vertical.
- Check whether the buyer is the clinician, the hospital administrator or the patient – the sales cycle is entirely different for each.
- Use the funding desk to see who actually led rounds in the last 24 months.
If you are buying or adopting
- Ask for the CE mark or equivalent clearance before anything else – an unregulated clinical claim is a red flag, not a growth stage.
- Request a reference site using the product in your specialty, not an adjacent one.
- Ask what data the vendor needs from your systems and how it is secured – integration and data governance kill more deals than price.
- Use the startup desk for a shortlist; use events for discovery, not for due diligence.
Who to know
Start on the desks – profiles update as we verify them
Glossary
Terms that keep coming up on this vertical
Latest coverage
Reporting and analysis tagged to this vertical
All verticals, by family
Twelve families – each carries its own icon and accent token
Frequently asked
About this vertical and how we cover it