Foundation Models
Tempus is your end-to-end partner to accelerate your AI strategy
Leverage our multimodal data and foundation models, deployed at scale.
One of the largest multimodal datasets in the world
~50 million unique cases across therapeutic areas, many with sequencing, imaging, and clinical histories
State-of-the-art foundation models and AI technology
Scientifically proven, multimodal foundation models and off-the-shelf tools accelerate and de-risk your AI development
Proven expertise developing clinical-grade AI
Bring AI models from initial proof-of-concept to robust, validated, and documented products suitable for the clinic
Regulatory excellence and track record
Multiple FDA authorizations across software (SaMD) and traditional diagnostics; dedicated regulatory team with extensive FDA and international expertise
Extensive deployment network and patient footprint
We operate at scale, reaching ~50% of US oncologists, with global infrastructure in place for broad AI deployment
Our models
State of the Art Foundation Models
We pioneered the Virchow and PRISM models, combining pathology images and clinical notes, setting the benchmark for foundation models in computational pathology.
Multimodal Foundation Model Expansion
We are building a unified foundation model that combines our data across modalities to develop a comprehensive understanding of the complexity of disease, beginning with oncology.
Future Vision for Foundation Models
As our dataset continues to scale, and we incorporate new data modalities, these modalities will be integrated into our foundation models, broadening capabilities and expanding to new disease areas.
Regulatory expertise
Navigate the regulatory landscape with our expertise across software and diagnostics
From AI-powered pathology to companion diagnostics, we provide end-to-end guidance to navigate submission and launch. Tempus has extensive regulatory experience inducing FDA approval for our xT CDx assay and 510(k) clearance for our xR IVD assay.
Software clearances
- Secured the first and only FDA de novo clearance for an AI-enabled pathology product, Paige Prostate Detect
- Gained multiple 510(k) clearances for AI-enabled algorithms, including ECG-AF and ECG-Low EF
- Earned two additional FDA Breakthrough Device Designations for Paige Breast Lymph Node and Paige PanCancer Detect
- Holds nine FDA clearances for its Pixel cloud-hosted viewer and applications
- Received 510(k) clearance for the FullFocus viewer, compatible with three major whole slide image scanners
- Obtained IVDR approval and 12 CE-IVD/UKCA marks covering 18 algorithms.
Traditional diagnostics
- Received FDA approval for its xT CDx assay and 510(k) clearance for its xR IVD assay.
- Regulatory affairs team of 10+ professionals with extensive FDA experience.
Our scale
Once AI-enabled diagnostics are developed, Tempus enables their deployment at scale
Partnership model
We offer flexible frameworks to align our AI capabilities with your needs
Access our technology off-the-shelf to enable your internal AI development
- License our pathology and multimodal foundation models to accelerate your development
- Access off-the-shelf AI tools, such as Paige Predict for biomarker prediction across 505 genes
Partner with us, from POC through commercialization on a customized project tailored to your unique needs
- Work together to build an new AI application or novel biomarker for your therapy
- Validate, deploy, and navigate complex regulatory submissions with our expertise
- Scale and drive clinical adoption through our extensive deployment network
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Research
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This is the future of healthcare.










