The Path To Cost Comparisons Can Go Through PCORI, Experts Say

While some seek creative means to leverage the recently created Patient Centered Outcomes Research Institute to encourage cost comparisons of technology and services, others say there are no real barriers to doing so.

As the Patient Centered Outcomes Research Institute gets up and running to drive the nation’s comparative-effectiveness-research agenda, some are seeking creative means to leverage the public-private entity to encourage cost comparisons of technology and services.

The 2010 health care reform legislation establishing the institute explicitly focuses on “clinical” comparative effectiveness research, rather than cost comparisons....

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Legislation

Medicare’s TCET Pathway Wins Acclaim From Early Users, Even As ‘Messy Middle’ Persists

 

Some of the first manufacturers to receive Medicare coverage for their breakthrough devices through the Transitional Coverage for Emerging Technologies pathway praise CMS’ engagement and timelines in the process, despite some challenges around post-launch data collection.

Medtech Industry Champions Smarter EU Environmental Rules

 

Europe’s medtech sector is actively supporting the European Commission’s push to cut red tape in environmental legislation. By offering practical solutions, the industry aims to ease regulatory burdens that have hindered innovation and competitiveness while maintaining patient safety.

Spanish Draft Bill Would Improve Clinical Research Use of Health Data

 

Spain is drafting a new digital health bill that aims to ensure the country is ready to implement the European Health Data Space Regulation.

House Bill Addresses ‘Valley Of Death,’ Establishes Medicare Coverage For Breakthrough Therapies

 

Bipartisan legislation pending in the US House aims to get FDA-designated breakthrough medical devices to patients with Medicare coverage more quickly.

More from Policy & Regulation

German Medtechs Choking Under EU Compliance And Reporting Obligations Tout Mutual Recognition

 
• By 

Industry survey points to ongoing low revenues rise and weaker profit levels for half of BVMed industry association members in 2025, as German manufacturers raise stakes on global harmonization.

Fixing The Fractures: New Aspirations For EU Medtech Regulatory Progress

 

A pioneering initiative, Edvance MedTech, is being launched by leading experts in medical technology regulation which aims get to the heart of what is needed to improve the way EU rules are not only applied but also decided.

MedTech Innovator Winner Armor Medical Hopes To Reduce 90% Of Preventable Maternal Deaths

 
• By 

Armor Medical’s wrist-worn wearable detected postpartum hemorrhage five times earlier than standard care in earlier studies. After surviving near-fatal hemorrhage herself, co-founder/CEO Kelsey Mayo aims to bring the device to market in 2028.