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A proposed collaboration with CBmed Ltd., Austria

Curious about the clinical potential
of your probiotic strain?

Identify the most relevant clinical application for your strain through our fully
integrated service offering

From strain characterization and candidate selection to clinical safety, efficacy, and
validation studies, our end-to-end support covers the full development pathway

What We Deliver

Strain Isolation

End-to-end strain isolation and characterization to identify the most promising probiotic candidates.

Strain Characterization

Targeted functional testing to demonstrate pathogen inhibition and immune-modulating potential.

Clinical Expertise

10+ years of expertise in probiotic research, from clinical guidance and method selection to protocol development.

Clinical Pilot Study

Pilot study solutions that generate early human data and support confident development decisions.

Clinical Gold Standard

Clinical validation programs using gold standard study setups, designed to deliver robust evidence for market-ready positioning.

Special Offer

We offer a no-cost initial test phase as a low-risk entry point for your team to assess our platform performance, scientific quality, and collaborative execution in a real project setting.

This entry phase is designed to generate early prioritization insights while establishing the basis for broader strategic collaboration.

In this introductory phase, we will:

  • Screen the indirect pathogen inhibition activity of one selected probiotic strain against 2 clinically relevant pathogens from our collection.
  • Demonstrate the quality, relevance, and reproducibility of our screening approach
  • Build confidence in our team, project delivery, and reporting standard

Proposed Timeline

NO COST Initital test phase (1-4 Weeks)

One selected probiotic strain against 2 clinically relevant pathogens

Strain Characterization (6-12 Months)

Understand the functional potential of your probiotic strain and define the clinical application

Clinical Exploration (1-3 Years)

Stepwise approach to de-risk development, safety, efficacy, validation studies

Get in touch

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