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NSA / IDR

NSA/IDR Clinical Value Dossier

Physician-authored dossier for No Surprises Act Independent Dispute Resolution proceedings. Every statutory factor addressed. Every arbitrator concern anticipated.

What IDR is

The No Surprises Act created a federal arbitration right for out-of-network payment disputes. The arbitrator reviews submissions from both parties and selects one offer — there is no middle ground. The quality of the clinical submission is the only variable entirely within the provider's control.

Clinovian addresses all six statutory additional circumstances with QPA analysis, clinical complexity narrative, and indexed exhibits. IDR disputes can be batched — multiple claims from the same payer, same CPT category, and same 30-business-day window submitted as a coordinated proceeding.

The six statutory factors
Factor 01

Provider training & experience

Board certification, subspecialty training, and quality/safety outcomes relevant to the disputed services.

Factor 02

Patient acuity & complexity

Clinical complexity, comorbidity burden, and severity markers that justify the billed amount relative to the QPA.

Factor 03

Teaching status & case mix

Teaching hospital designation, case mix index, and the resource intensity associated with the practice setting.

Factor 04

Good faith demonstrations

Prior contracting attempts, negotiation history, and evidence of efforts to reach agreement.

Factor 05

Prior contracted rates

Historical rate evidence if prior contracts existed between the parties.

Factor 06

Market rate benchmarking

Geographic, specialty, and complexity-adjusted benchmarks that contextualize the provider's offer relative to market rates.

Get started

IDR is the fastest path to a measurable result.

Per-case engagement. No long-term contract. The determination timeline is measurable.

3,000+ Cases Reviewed
Free Suitability Screen
Fixed Per-Case Fee
BAA Before Records
Criteria-Mapped Logic