Part D in Peril: The Inconvenient Math of IRA Part D Redesign 

Home / Intelligence / Webinars / Part D in Peril: The Inconvenient Math of IRA Part D Redesign 

August 14, 2025 | 12:00 - 12:45 PM ET

Two additional sessions will be offered:
August 18 – 12:00 – 12:45 (UTC +8:00) – Asia
August 18 – 12:00 – 12:45 CET – Europe/Berlin 

Medicare Part D is undergoing its most significant transformation in decades largely driven by the Inflation Reduction Act (IRA). What does this mean for pharmaceutical manufacturers? 

Join us for an engaging discussion with Max Hunt, Partner at Trinity Life Sciences, and special guest Dan Simenc, clinical and actuarial expert at Milliman, as they provide perspectives on recent developments and future expectations for Medicare Part D and Medicare Advantage. The webinar will explore trends in drug spending, the impact of the IRA Part D redesign, learnings from the latest cycle of negotiations and implications for manufacturers. 

Whether you’re launching a new therapy or managing an innovative drug, gain the insights you need to stay ahead in the dynamic payer and policy landscape in the U.S.

Key Webinar Topics

  • Drug spending trends in 2024 and 2025 to date, including the impact of the IRA Part D redesign 
  • Learnings from the most recent cycle of manufacturer and Medicare Advantage/Part D negotiations for 2026
  • Expectations for access to Medicare Advantage and Part D for innovative drugs and new launches in the next 2-3 years 
  • Implications for manufacturers of innovative drugs on the market and those that will launch in this period 

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Which session would you like to attend?

Complete the form below to register for the August 14th session at 12:00 PM ET

Complete the form below to register for the August 18th session at 12:00 UTC+8 – Asia

Complete the form below to register for the August 18th session at 12:00 CET – Europe/Berlin

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