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    Generative AI assistant grounded in clinical data with cited sources
    Generative AI for Healthcare

    Generative AI for healthcare, grounded in your clinical data

    We build retrieval-augmented (RAG) systems over clinical data — summaries, drafting, and Q&A grounded in the actual record, with PHI guardrails, citations back to source, and human review on anything clinical.

    HIPAA-ReadyGrounded RAGCited OutputHuman Review

    Trusted by global innovators

    Benchmark
    Chibasco
    Fundency
    Lantimer
    Lauren
    Lera
    One Minute
    Pento Pix
    TAP
    Xtrium
    Healthevolve
    Benchmark
    Chibasco
    Fundency
    Lantimer
    Lauren
    Lera
    One Minute
    Pento Pix
    TAP
    Xtrium
    Healthevolve
    Benchmark
    Chibasco
    Fundency
    Lantimer
    Lauren
    Lera
    One Minute
    Pento Pix
    TAP
    Xtrium
    Healthevolve
    Benchmark
    Chibasco
    Fundency
    Lantimer
    Lauren
    Lera
    One Minute
    Pento Pix
    TAP
    Xtrium
    Healthevolve

    Generative AI that's grounded, not hallucinated

    The healthcare value of generative AI is real — summarizing a long chart, drafting a patient-friendly discharge note, answering 'what's this patient's cardiac history?' in seconds. The risk is equally real: a model that confidently invents a medication or a lab value is worse than no model at all. The difference is grounding.

    We build retrieval-augmented generation (RAG) over your clinical data: the model answers only from retrieved, permissioned source documents, cites the spans it used, and abstains when the record doesn't support an answer. Every generation runs behind PHI guardrails and, for anything clinical, a human-in-the-loop review step. That's the line between a demo and a system you can deploy.

    What it is

    Generative AI, constrained to the record

    Generative AI for healthcare uses large language models to summarize, draft, and answer questions — but constrained by retrieval so the output is grounded in your actual clinical data rather than the model's training set.

    The engineering that matters is retrieval quality, PHI guardrails, citation, abstention, and human review. We build all of it, and we measure faithfulness rather than trusting a good demo.

    A reference architecture for clinical generative AI

    Retrieval, PHI guardrails, grounded generation with citations, and a review layer — assembled so you can defend every output to compliance and to clinicians.

    Clinical RAG architecture with retrieval, guardrails, and cited generation

    What we build into a clinical GenAI system

    Each capability pairs a generative feature with the guardrail that makes it safe to ship.

    15-Minute Scoping Call

    Retrieval-Augmented Generation (RAG)

    Answers are grounded in retrieved clinical documents via a vector store and hybrid search over FHIR resources and notes, so the model draws from the real record instead of its training data.

    Clinical Summarization & Drafting

    Chart summaries, visit recaps, referral letters, and patient-friendly instructions — each generation carries citations back to the source span so a clinician can verify before signing.

    PHI Guardrails & Access Control

    Prompt and output filtering, per-user data scoping, de-identification where full PHI isn't needed, and BAA-covered model hosting so no PHI leaks into a public endpoint.

    Grounding, Citations & Abstention

    The system cites the exact documents it used and abstains when retrieval doesn't support an answer — hallucination is engineered against, not hoped away.

    FHIR-Aware Retrieval

    Retrieval spans structured FHIR R4 resources and unstructured notes, so a summary reflects both the coded record and the narrative — not one at the expense of the other.

    Evaluation & Human-in-the-Loop

    Faithfulness, groundedness, and safety are evaluated against curated test sets, and clinical output routes through review before it reaches a chart or a patient.

    Where it runs

    Generative AI use cases

    Chart summarization

    Condense a long record into a clinician-ready synopsis with citations.

    Ambient note drafting

    Draft structured notes for clinician review and sign-off.

    Patient communication

    Plain-language discharge and instruction drafts at the right reading level.

    Prior-auth support

    Assemble and draft supporting documentation from the record.

    Clinical Q&A

    Answer questions about a patient grounded in their own data.

    Coding & documentation assist

    Suggest codes and surface documentation gaps for review.

    Where generative AI pays off in healthcare

    Grounded summarization and drafting save clinician time — but only when hallucination is engineered against and a human stays in the loop.

    0
    PHI sent to non-BAA public endpoints
    100%
    clinical generations carry source citations
    Review-gated
    output before it reaches a chart or patient

    Compliance-First Healthcare App Development Services Backed by Global Standards

    15-Minute Scoping Call
    01HIPAA logo

    HIPAA

    Health Insurance Portability and Accountability Act

    Protect PHI with privacy-first architecture, encrypted storage and transmission, strict access controls, and traceable audit logs.

    02GDPR logo

    GDPR

    General Data Protection Regulation

    Implement lawful consent flows, data minimization, retention controls, and secure processing for sensitive health data.

    03FHIR logo

    FHIR

    Fast Healthcare Interoperability Resources

    Enable standardized health data exchange across apps, care teams, and systems through robust FHIR-ready APIs.

    04HL7 logo

    HL7

    Health Level Seven International

    Support enterprise-grade interoperability with HL7-based integrations for records, events, and clinical messaging workflows.

    05HITRUST logo

    HITRUST

    Health Information Trust Alliance

    Align security programs to healthcare-specific control and risk management practices trusted by providers and ecosystem partners.

    06HITECH logo

    HITECH

    Health Information Technology for Economic and Clinical Health Act

    Design with breach notification readiness, digital record safeguards, and operational controls that support regulated care programs.

    07SaMD logo

    SaMD

    FDA Software as a Medical Device

    Plan software quality, traceability, and documentation pathways for products that may require SaMD review and submission.

    08MDR (EU) logo

    MDR (EU)

    Medical Device Regulation (European Union)

    Prepare EU market-ready processes for risk classification, evidence tracking, and lifecycle governance under MDR expectations.

    09SAMHSA logo

    SAMHSA

    Substance Abuse and Mental Health Services Administration

    Apply confidentiality controls and consent-aware sharing models for behavioral and mental health data experiences.

    Standards we build against

    Standards and controls in our GenAI stack

    FHIRHIPAAHITECHSOC 2SNOMED
    Our Process

    From promising demo to deployable system

    We treat evaluation and guardrails as the hard part of clinical GenAI — because they are.

    1.

    Use-Case & Risk Framing

    We pick a use case with clear value and bounded risk, define what 'correct' means, and decide where a human must stay in the loop.

    Risk-framed
    2.

    Retrieval & Grounding Build

    We build the RAG pipeline over your clinical data — chunking, embeddings, hybrid retrieval, and citation tracking across FHIR resources and notes.

    Grounded RAG
    3.

    Guardrails & Evaluation

    PHI filtering, abstention behavior, and a faithfulness/groundedness eval harness so quality and safety are measured against real test cases.

    Measured safety
    4.

    Deploy with Review

    Human-in-the-loop review for clinical output, BAA-covered hosting, and monitoring for drift, cost, and hallucination signals in production.

    Audit-ready

    Featured case study

    Read Case Study

    Lera Health: compliant women's health platform

    Lera Health demonstrates our approach to turning clinical inputs into trustworthy, personalized output within a privacy-first data layer — the same foundation that makes generative AI safe to deploy in a regulated setting.

    Lera Health app across desktop and mobile
    Why Partner With Us

    Generative AI you can put in front of clinicians

    We build for grounding, safety, and audit — the properties that separate a healthcare GenAI product from a risky demo.

    15-Minute Scoping Call

    Guardrails-First

    PHI filtering, grounding, and abstention are designed in from the first prototype, not patched after a bad output.

    Grounded, Not Generic

    RAG over your real clinical data with citations, so answers reflect the patient in front of you — not the internet.

    Human-in-the-Loop by Design

    Clinical output routes through review, and we build the workflow that makes that fast rather than a bottleneck.

    Clinical-Domain Depth

    We understand where generative AI helps and where it must never be trusted unattended.

    Our relevant experience

    Generative AI that survives a compliance review

    Frequently Asked Questions

    We use retrieval-augmented generation so the model answers only from retrieved source documents, cites the spans used, and makes the system abstain when the record doesn't support an answer. We then evaluate faithfulness against a curated test set. Hallucination is engineered against and measured, not left to chance.

    Ready to deploy generative AI you can defend?

    Tell us the workflow you want to accelerate. We'll return a grounded, guardrailed design with an evaluation plan and a human-in-the-loop approach.

    Email

    contact@agnotic.com

    Partnerships

    contact@agnotic.com