CMS-0057-F: What’s Changing Next
CMS is closing the gaps in prior authorization with more automation, stronger standards, and greater transparency—across all drugs, all programs, all payers.
The Big Picture: CMS Is Closing the Gaps
More Automation
Electronic prior authorization becomes the default.More Transparency
Stronger reporting and visibility into PA performance and outcomes.More Standardization
Consistent digital workflows and interoperability standards.More Accountability
Consistent reporting across payers and programs.Key Updates in the Proposed Rule
Electronic PA Expands to Include Drugs
- Electronic PA required for all drugs.
- Medical benefit drugs via electronic PA.
- Pharmacy benefit drugs via established pharmacy standards.
Two Standards, Depending on Drug Type
- FHIR for medical benefit drugs.
- NCPDP for pharmacy benefit drugs.
- Plans must manage two parallel workflows.
More Transparency & Reporting Requirements
- Report API usage metrics.
- Publish PA performance and drug-related metrics.
- Provide detailed denial reasons.
- Track approvals, denials, and extensions.
APIs Become More Central to Everything
- Patient Access, Provider Access, Payer-to-Payer, Prior Authorization, and Provider Directory APIs.
- Expose status, timelines, denial reasons, approved drugs, dosage details, and supporting clinical documentation.
Standardization Is Tightening Again
- Move to updated, non-expired FHIR standards.
- More implementation guides become required.
- Older standards like X12N 278 phase out over time.
Endpoint Transparency Is Mandatory
- Payers must report API endpoints and technical details.
- CMS will publish endpoint information centrally.
- Connections become easier for providers, vendors, and developers.










