Precision medicine and data
Prenosis Sepsis ImmunoScore
FDA De Novo-authorized AI/ML software that assigns adult emergency department or hospital patients to sepsis risk categories within a clinician-reviewed workflow.
Last updated: June 5, 2026
Back to directoryTempus medical AI product profile
AI-enabled precision medicine platform spanning molecular testing, multimodal data, clinical assistants, care pathways, imaging insights, and trial matching.
Precision medicine and data
Best fit
Oncology and life-sciences teams evaluating AI-enabled precision medicine workflows that combine molecular, clinical, imaging, and real-world data.
- Primary use case
- AI-enabled precision medicine, multimodal data, diagnostics, and clinical trial support
- Audience
- Oncology, cardiology, radiology, life-sciences, and precision-medicine teams
- Risk level
- High
- Pricing signal
- Enterprise, clinical, and life-sciences pricing; request current terms.
- Official sources
- 5 official sources
Compare within workflow: Precision medicine and data · comparison shortlist · source index
Regulatory, privacy, evidence, and workflow lens
Product-specific review. These product-specific signals summarize what the cited sources imply before treating Tempus as safe for a local clinical, operational, or research workflow.
| Regulatory / FDA | Separate molecular assays, companion-diagnostic claims, EHR assistants, imaging algorithms, trial matching, and care-pathway notifications because each workflow can carry different regulatory and clinical accountability. |
|---|---|
| Privacy | Review whether data is handled under website privacy, notice-of-privacy-practices, customer contract, research agreement, or de-identified data program before connecting EHR, genomic, imaging, or real-world datasets. |
| Evidence | Require product-level validation for the disease area, data type, model output, and care setting rather than relying on broad precision-medicine platform positioning. |
| Workflow | Map how outputs enter tumor boards, EHR workflows, trial screening, imaging review, care-gap closure, or life-sciences analysis, and define who approves downstream actions. |
Where Tempus fits
Tempus describes an AI-enabled precision medicine platform with Tempus One, Hub, Lens, Pixel, Next Pathways, Next Trials, assays, and algorithms; official technology and privacy pages should be checked for product-specific clinical, lab, data, and PHI boundaries.
Not for: Simple chatbot-style medical questions, autonomous treatment selection, or using platform-level AI claims without product-specific validation and clinician review.
What to verify before using Tempus
- Which Tempus product is in scope: One, Hub, Now, Lens, Pixel, Next Pathways, Next Trials, assays, or algos.
- Product-specific clinical, laboratory, FDA/CDx, and EHR-integration status for the exact workflow.
- Data provenance, consent, de-identification, PHI handling, and privacy-policy or notice-of-privacy-practices applicability.
- How AI outputs affect treatment, trial matching, care-gap notifications, image quantification, diagnosis workflows, and accountable clinical review.
Source links
Use these links to confirm current claims, terms, regulatory status, pricing, and deployment requirements.
- www.tempus.com
- www.tempus.com / about-us / tempus-tech
- www.tempus.com / about-us / tempus-tech
- www.tempus.com / privacy-policy
- www.tempus.com / tempus-privacy-and-compliance-policies
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