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Intelligent UM. The closed loop UM was missing.

Prior auth, concurrent, retro, appeals, and grievances on one Operating System. Documentation hunting, criteria lookups, and evidence assembly come off your clinicians' desks. Every recommendation arrives at the reviewer's queue with the time-consuming work already done.

The problem

The playbook you've been handed.

Health plans have been trained to scale UM the same way for decades. Add headcount when volume rises. Buy a tool when a workflow breaks. Layer governance on top of fragmented systems. It made sense when volumes were predictable and regulators were patient. Neither is true anymore.

By the time it's all stood up, you don't have a UM strategy. You have a stack of vendors, a hiring pipeline that cannot keep up, and a medical director queue that grows faster than it clears.

Here's where it breaks: the model assumes UM is a staffing problem. It is a system problem that staffing has been asked to solve. Every reviewer you hire enters the same broken workflow, with the same inconsistent criteria application, and the same documentation gaps. The bottleneck moves to the next person. The administrative burden stays the same.

  1. 01

    Volume rises.

    PA requests, concurrent reviews, retro intake, appeals. All climbing.

  2. 02

    Hire more reviewers.

    Slow, expensive, and the clinical talent pool is shrinking.

  3. 03

    Buy a point solution.

    A tool for prior auth. Another for appeals. Another for grievances. Each with its own queue.

  4. 04

    Repeat.

    Every quarter. Every audit cycle. Every regulatory update.

The real cost

It is not just the headcount budget. It is what happens between the seams.

When prior auth, concurrent review, retro, and appeals all live in separate systems, the same case gets re-evaluated three times by three different teams who cannot see each other's work. That is an operating model problem that point solutions have created and then sell you more software to manage.

Clinical reviewer hours

Spent on documentation hunting and criteria lookups instead of clinical judgment. Highly trained nurses and physicians orienting to cases instead of evaluating them.

Inconsistent recommendations

On clinically identical cases, driving appeal volume that compounds quarter over quarter.

Audit exposure

When documentation trails are incomplete and rationale lives in a reviewer's head, not in the record. CMS, NCQA, URAC, and state regulators have all tightened the standard.

The lightbulb

Every appeal is a signal. Right now it is being ignored.

There is a moment when it clicks. Health plans stop asking "how do we staff up appeals?" and start asking "why is this volume here in the first place?" The answer is the same every time. Criteria are being applied inconsistently at intake. Documentation gaps are not being caught until after the recommendation has issued. And nothing in the current stack closes the loop between what gets overturned at appeal and what gets reviewed at prior auth tomorrow morning.

Engine 01

Prospective review.

Apply criteria consistently before the recommendation issues.

Closed loop

Engine 02

Retrospective recovery.

Appeals, IRO, and grievances handled end-to-end with every outcome captured and routed back.

Each appeal outcome and retrospective finding feeds back to prospective review so the same gap does not repeat.

Prospective review

Intake through recommendation.

Catch documentation gaps and apply criteria consistently before the recommendation reaches your medical director. Cases arrive at the reviewer with rationale documented, criteria mapped, and evidence organized.

  1. 01

    Intake.

    Requests received from provider portals, fax, EHR integrations, or direct API. Clinical documentation extracted and organized. Zero manual data entry by UM staff.

  2. 02

    Queuing.

    Cases prioritized by urgency, regulatory deadline, and plan type. Workload distributed across staff based on capacity and case type so reviewers get the right cases at the right time.

  3. 03

    Criteria application.

    Medical necessity criteria, evidence guidelines, and proprietary plan criteria applied consistently. Documentation gaps identified before the case reaches your reviewer.

  4. 04

    Prior authorization.

    Standard cases prepared with full rationale documented. Denial-track cases arrive at your medical director's queue ready to issue. Complex cases surfaced with evidence already mapped to criteria.

  5. 05

    Concurrent review.

    Inpatient and outpatient stays monitored in real time. Length-of-stay criteria applied continuously as clinical status evolves. Post-acute transitions, observation validation, and SLA tracking handled within the same workflow.

  6. 06

    Human review.

    Your reviewer accepts, modifies, or overrides every recommendation. The clinical judgment belongs to your team. Nothing issues without your clinician's sign-off.

Retrospective recovery

Appeals, grievances, and IRO coordination end-to-end.

Post-service review, appeals, and grievances handled in one workflow. Every outcome captured. Every signal routed back to the front end.

  1. 01

    Retro intake.

    Post-service documentation reviewed from intake through final disposition. Retro exception logic applied. Criteria matched. Adjudication recommendations prepared with complete supporting evidence.

  2. 02

    Appeals routing.

    First-level, second-level, and IRO coordination handled within a single workflow. Cases routed by complexity, regulatory deadline, and plan requirements.

  3. 03

    Evidence assembly.

    New clinical evidence identified and analyzed against the original recommendation. Documentation gaps flagged. Criteria re-applied with full traceability.

  4. 04

    Recommendation preparation.

    Appeal recommendations and supporting rationale assembled. Medical directors receive cases with evidence mapped and clinical context organized for their review.

  5. 05

    Grievance handling.

    Member grievances logged, categorized, and routed with full documentation. Regulatory timelines tracked at every stage.

  6. 06

    IRO coordination.

    External review packets assembled. Communication tracked. Outcomes captured and reconciled.

  7. 07

    Outcomes.

    Every appeal outcome and grievance resolution captured. Patterns identified. Quality and financial impacts reconciled.

  8. 08

    Feedback loop.

    Root cause of every overturned recommendation routed back to prospective review. Each appeal outcome strengthens the next intake. The system gets smarter every cycle.

How this is different

Four things your current stack cannot give you.

The loop is closed.

Every overturned appeal teaches prospective review how criteria are being applied and where documentation gaps repeat. The two engines make each other smarter. Your current vendors cannot do this. They do not talk to each other.

One Operating System, every UM workflow.

Prior auth, concurrent, retro, appeals, grievances, IRO. All on one Operating System. No point-solution stitching. No reviewer toggling between four systems to evaluate one case. No queue handoffs where context gets lost.

Your clinicians practice the art of medicine.

Reviewers and medical directors see exactly how every recommendation was reached and apply their clinical judgment. The Ai Workers handle documentation extraction, criteria matching, and evidence assembly. Your team gets back to the work their training is for.

Your systems stay yours.

Your core admin platform stays the system of record. Provider portals stay the intake path. Nothing issues without clinical approval. No rip-and-replace. No parallel infrastructure to manage.

Enterprise governance built for health plans

Every recommendation, explained. Every action, logged.

Health plans operate under CMS, NCQA, URAC, and state regulatory frameworks. Trust and accountability are not optional. Penguin Ai was built with governance as a structural requirement.

  • The Glassbox

    Every recommendation surfaces the criteria applied, the clinical data reviewed, and the reasoning behind it. Your medical directors verify, stand behind, and present every recommendation to any regulator or IRO with confidence.

  • Full audit trail

    Every recommendation, denial draft, and appeal action documented with clinical reasoning, criteria applied, and data sources referenced. Regulatory review-ready at all times.

  • Regulatory turnaround compliance

    Statutory and contractual timeframes tracked automatically across Medicare Advantage, Medicaid, and commercial lines. Deadlines met without manual monitoring.

  • Configurable plan-specific criteria

    Medical necessity criteria, evidence guidelines, and proprietary plan criteria applied consistently with no workarounds or manual lookups.

  • Human in the loop

    Penguin Ai and your clinical staff work in tandem. The Ai Workers prepare the work. Your reviewers and medical directors apply their expertise and make the call.

  • Continuous learning

    Every appeal outcome and reviewer override strengthens future recommendations across prospective and retrospective workflows.

The next time someone tells you the answer to your UM backlog is more reviewers or another point solution, ask what that actually delivers for members waiting on authorizations and clinicians buried in documentation this week.

UM should give your clinical staff their time back. It should give your medical directors recommendations they can stand behind. It should give your members responses at the speed of human need.

See it in action

Show us the worst part of your UM operation.

A Penguin Ai specialist will walk through exactly how the closed loop runs against your appeals backlog and prior auth queue, with your data.