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CMS Needs Payment Reform Ideas For Rare Diseases From Private Sector – Former Official

 
• By Cathy Kelly

Speaking to a DIA/NORD conference, former Center for Medicare and Medicaid Innovation official William Shrank agreed that the agency’s current experiments in payment reform are not designed to accommodate rare disease patients.

The biopharmaceutical industry and patient advocacy groups should develop ideas for tailoring federal government payment reforms to rare disease patients and present them to CMS, suggested William Shrank, former director of rapid-cycle evaluation at the agency’s Center for Medicare and Medicaid Innovation.

Speaking to the DIA/NORD conference on rare disease and orphan products Oct. 9, Shrank agreed that current experiments in government reimbursement reform are not designed specifically to accommodate the needs of rare disease patients. He also acknowledged the need for casting a wide net, both in the U.S

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