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Last updated: June 5, 2026
Back to directoryTempus generative AI assistant for querying clinical, molecular, imaging, EHR, and research data inside precision-medicine workflows.
Oncology and precision-medicine teams that need governed access to Tempus patient insights, test status, guideline context, trial matching, and multimodal data summaries.
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Product-specific review. These product-specific signals summarize what the cited sources imply before treating Tempus One as safe for a local clinical, operational, or research workflow.
| Regulatory / FDA | Treat as high-risk precision-medicine decision support and workflow automation; separate clinical reference, documentation, prior authorization, trial matching, cohort research, and order-related use because each can carry different regulatory, contractual, and clinician-accountability obligations. |
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| Privacy | Review Tempus privacy and compliance terms, customer agreements, EHR integration scope, PHI flows, support access, retention, audit logging, cross-product data use, and whether custom agents can access institution-specific procedures or repositories. |
| Evidence | Validate every guideline, biomarker, trial, patient-history, and cohort output against the underlying Tempus report, EHR note, guideline source, source excerpt, or research dataset before relying on it clinically. |
| Workflow | Best governed as clinician- or researcher-reviewed assistive infrastructure with local rules for source checking, note editing, prior-authorization review, trial-screening confirmation, patient communication, and custom-agent change control. |
Tempus describes Tempus One as a generative AI-enabled assistant for healthcare providers and researchers that can surface patient insights from clinical and molecular data, support EHR workflows, summarize histories and biomarkers, search trials, and process unstructured multimodal data; Tempus announcements also describe EHR integration, guideline access, documentation support, and custom agent-building capabilities.
Not for: Autonomous treatment selection, unsupervised patient communication, unsupported specialties, or use outside validated Tempus data, EHR, and institutional governance boundaries.
Use these links to confirm current claims, terms, regulatory status, pricing, and deployment requirements.