Master Complex Regulatory Guidelines to Deliver Compliant Government Pricing and Reporting Programs
Thank you for spending time with us at Medicaid Drug Rebate Program Summit
This page highlights selected content and resources that connect to the issues shaping pharmaceutical pricing and contracting today, including effectuating Maximum Fair Prices (MFPs), gross-to-net pressure, and government pricing — areas where small methodology choices and process gaps translate directly into financial exposure, compliance risk, and lost margin.
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From the Pricing and Contracting 2026 stage: Presentation
Post First Quarterly ASP Submission Review of Physician Fee Schedule Final Rule

This session offered a candid look at the implementation challenges that surfaced under the updated Physician Fee Schedule Final Rule, practical guidance on compiling documentation that holds up, and step-by-step approaches to building standardized processes and quality controls that make future submissions cleaner.

Lifecycle-based GTN

Gross-to-net can shape commercialization strategy as much as it shapes financial reporting, but many life sciences teams still treat it as a back-office exercise. This guide breaks down where Gross-to-Net models go wrong, how to build more adaptable forecasting, and what lifecycle-based support can look like in practice.

Medicaid Final Rule Reference Guide

Stay ahead of the curve on the Medicaid Drug Rebate Program’s Final Rule, which takes effect on November 19, 2024, using our comprehensive white paper packed with valuable insights on what provisions could impact different manufacturers and key operational and financial factors to consider.

Our Latest Thinking
Strategies for Specialty Pharma to Navigate Government Pricing

This piece explores key risks of pricing specialty therapies — from gross-to-net forecasting and inflation penalties to value-based agreements, IRA impacts, and state transparency laws — and shows why strategic government pricing can become a competitive advantage.

Our Presentation
Approaches and Considerations for Effectuating MFP

This presentation from Riparian and King & Spalding covers approaches for effectuating MFP: core program requirements, choosing between prospective and retrospective access models, Effectuation Plan deadlines, and a realistic timeline for implementing by 2028.

Continue the conversation
Explore our latest thinking on the complex challenges shaping the future of healthcare.

If you’d like to continue the conversation or learn more about how Riparian supports pricing for biopharma manufacturers, we’d be glad to connect.

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