AI Diagnostics

Waiv products

Clinically validated digital pathology AI to augment precision oncology workflows

Transform image into action with AI diagnostics

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Significant patterns revealed at the tissue level
Lymphocytes - after
Lymphocytes
H&E
Lymphocytes

Our products enhance patient diagnostics in 3 key ways:

Biomarker Screening
Screen biomarkers

Prioritize patient cases for further molecular tests by predicting those most likely to have the biomarker.

MSIntuit Report
Predict outcomes

Analyze the likelihood of survival, relapse, and response to treatment to better inform targeted treatment options.

Digital Pathologist
Support pathologists

Provide quick and standard interpretation of H&E or IHC Whole Slide Images (WSIs).

RlapsRisk: Next-generation AI testing from routine H&E to inform the treatment pathway for early breast cancer patients
Best in class

Groundbreaking AI diagnostics, accessible across diverse workflows and IT settings

Pictured above: RlapsRisk BC results in action. Image for presentation only.
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Faster than existing tests

Minutes vs. weeks.

Scalable Icon
Scalable

Software that runs on standard oncology data.

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Seamless integration

Platform agnostic and plug-and-play.

Cost saving
Cost saving

Compared with traditional tests.

Tissue sparing
Tissue sparing

Multiple analyses possible with same tissue sample.

Standardized reports
Reproducible

Standardized reports at the click of a button.

Our building blocks for robust diagnostics

Our vast patient data network lays the foundation for impactful products that meet critical medical needs.
81

Eighty-one leading academic institutions and pathology labs with secured data access.

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Thirteen countries that ensure diverse cohorts.

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Thirty-three therapeutic indications in oncology, immunology and inflammation, with leading KOLs in each field.

We are a world leader in AI and machine learning for digital pathology.
Interpretable

Breakthrough models built on a foundation of 8+ years of R&D with 59 tier 1 peer-reviewed articles.

Generalizable

Maximizing performance and generalizability with world-class foundation models and expertise in model fine-tuning.

Validated

Products undergo robust multicentric and international validations, across a variety of hardware and IT settings.

Waiv has regulatory proficiency in navigating the new CE-IVDR and FDA frameworks.
Regulatory expertise

In-house quality management and niche experience in developing AI as fully approved IVDs for clinical use.

International security standards

Robust infrastructure to obtain and maintain ISO certifications.

Notified bodies

Audited by French health authorities certified (ANSM). GMED is our notified body.

Get in touch

Ready to accelerate your biomarker program?

Whether you’re exploring early translational questions or planning a full CDx co-development, our team is ready to discuss how Waiv can support your program.