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TwinFyRx Labs

From plan restrictions to
access friction intelligence

Walk through five transformations that turn raw CMS Part D formulary data into composite access friction scores. See how prior auth, step therapy, and quantity limit signals combine to reveal payer access barriers.

Step 1 of 5

Plan-Level Restrictions

Raw Part D formulary data

Every Part D plan publishes which drugs it covers and what restrictions apply. CMS aggregates these into quarterly public-use files. Each row is a plan × drug combination with tier placement and access control flags.

ContractPlanDrugTierPASTQLQL Detail
H0028007Humira 40 mg pen56 per 28 days
H0028007Ozempic 1 mg pen33 per 28 days
H0028007Eliquis 5 mg tablet374 per 30 days
H0028007atorvastatin 20 mg1—
S2893001Humira 40 mg pen56 per 28 days
S2893001Ozempic 1 mg pen33 per 28 days
S2893001Eliquis 5 mg tablet374 per 30 days
S2893001atorvastatin 20 mg130 per 30 days
R0110003Humira 40 mg pen56 per 28 days
R0110003Ozempic 1 mg pen33 per 28 days
R0110003Eliquis 5 mg tablet374 per 30 days
R0110003atorvastatin 20 mg1—
Prior Auth Step Therapy Quantity Limit
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Real 2026 plans, one of each type (MA-PD, PDP, Regional PDP): Humira 40 mg pen (Tier 5) needs prior auth in every plan; Ozempic 1 mg pen (Tier 3) needs prior auth in every plan; Eliquis 5 mg tablet (Tier 3) needs no prior auth; atorvastatin 20 mg (Tier 1) needs no prior auth. The raw data already tells a story about access difficulty.