FD/MAS Registry Working Group

A Rare Bone Disorder Registry

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Articles from December 2015

Comparative Effectiveness Research – Seeking input from all stakeholders
December 17, 2015 Deanna Portero

The Fibrous Dysplasia/McCune-Albright syndrome (FD/MAS) Patient Registry Working Group will attend a series of meetings held during the week of 12/14. These meetings will educate Working Group members on comparative effectiveness research (CER), and engage the many stakeholders of the Working Group to provide ideas related to the types of

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Recent Posts

  • Fibrous Dysplasia Foundation and NORD Launch Cutting-Edge Study of Fibrous Dysplasia/McCune-Albright Syndrome
  • FD/MAS Patient Registry Gains New Support from Influential Patient Group
  • PCORI Announces $25,000 Tier II Award for Project
  • Fibrous Dysplasia Foundation Interviews FD/MAS Patient Registry Project Lead
  • CER Meeting – Updates and Highlights

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