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Industries · HEALTHCARE

Healthcare funding, handled.

Devices, diagnostics, digital health and medical software carry deep R&D and long timelines. We secure the funding that de-risks the path from prototype to clinic.

What we fund

Long development cycles, strong funding fit

Healthcare development is R&D-intensive by nature: devices, diagnostics, digital health, sensing, signal processing, software, validation and trials all qualify. Non-dilutive funding extends your runway through the parts that take the longest.

Why this industry

Why R&D funding fits Healthcare

Four reasons healthcare companies are well positioned for German R&D funding.

Years

Long, fundable development cycles

The years of development and validation before market entry are exactly the period the Research Allowance is built to support.

2024

Equipment counts too

Since 2024, depreciation on machines and equipment used directly in an R&D project can be included in the eligible base, which matters for device and lab-heavy work.

Wages

High-skill, high-cost teams

Funding is built around R&D wage costs, and healthcare teams are full of the engineers, scientists and specialists those costs cover.

EU

Strong EU pull

The Horizon Europe health cluster (Cluster 1) and the EIC actively fund medical innovation, giving healthcare teams a route to larger grants on top of the national instruments.

Eligible activities

What healthcare activities qualify

Four categories of healthcare R&D that consistently qualify. The common thread is technical uncertainty.

Medical devices

  • New device development from concept through functional prototype
  • Design and engineering to resolve a problem with no standard solution
  • Verification and validation testing requiring systematic experimentation

Diagnostics and assays

  • New in-vitro diagnostic methods, assays and biosensors
  • Analytical method development and validation under uncertainty
  • Sensitivity, specificity and reproducibility studies for a novel method

Digital health and SaMD

  • Image analysis, signal processing or decision-support algorithms
  • ML models for diagnosis or risk prediction developed from the ground up
  • Software as a medical device carrying genuine technical risk

Lab and process development

  • New laboratory methods, workflows and automation
  • Scale-up of a process from bench to reproducible production
  • Materials and biocompatibility development for a device or assay
What qualifies and what doesn't

The line that decides a claim

The line that decides a claim is technical uncertainty. A quick orientation for healthcare:

Usually qualifies

  • Device, diagnostic or SaMD development resolving technical uncertainty
  • Preclinical and bench work, including Class III clinical investigation
  • Validation methods for a novel device or assay

Usually does not

  • Clinical evaluation of Class I to IIb devices and IVD performance evaluation
  • Regulatory approval, certification and DiGA listing on their own
  • Routine medical care and standard quality control
Indicative ranges

How much healthcare companies typically receive

Indicative ranges based on R&D team size and intensity. Actual figures depend on eligible costs and the funder's decision.

Early-stage healthcare
€80k – €250k

Mostly the Research Allowance on a core development and validation team.

Growing healthcare
€250k – €900k

The Research Allowance stacked with a ZIM grant on a defined development project.

Established / diagnostics
€900k – €4.2M

Toward the Research Allowance ceiling, plus stacked ZIM and Horizon Europe health funding.

* Indicative figures. The actual amount depends on company size, eligible costs and the programs you qualify for.

Typical eligible work

The kind of healthcare work that qualifies

If it carries genuine technical risk and novelty, it usually counts. A few examples:

Device and sensor development

Sensor fusion, signal processing and hardware prototyping for diagnostics or therapy.

Medical software and algorithms

Clinical decision support, imaging and AI models with technical novelty.

Validation and testing

Bench testing and pre-clinical work that resolves technical uncertainty.

Process and manufacturing R&D

New production or quality methods for regulated medical products.

FAQ

Healthcare funding, answered

The R&D and validation work that resolves genuine technical uncertainty can qualify. Pure regulatory administration does not, but the development and systematic testing behind it often does. We help you separate the two.

Yes. The Research Allowance is paid out even with no profit, which suits the long pre-market period typical in healthcare.

Since 2024, depreciation on machines and equipment used exclusively and directly in an R&D project can be included in the eligible base. We assess which of your equipment qualifies.

Yes. Contract research is eligible at 70% of the cost, so working with a university or institute does not exclude you, it adds to the eligible base.

The Research Allowance and ZIM cover the national base, while Horizon Europe (Cluster 1) and the EIC fund larger, more ambitious programmes. We design the stack so they reinforce each other.

Talk to us

Ask us anything

Tell us about your project and we'll assess your case by hand. No prep, no obligation. Prefer to talk?