Assistance with MIPS reporting is a significant draw to the registry, and it also serves an essential function in research and development in the rheumatology field. The registry already has data from more than 16 million patient encounters. These data are now being used in research projects to better understand rheumatic diseases and improve patient care. More than 50 projects have been initiated using RISE data, leading to 22 publications.
Are you interested in joining RISE? Check out the RISE registry website for more information, or email [email protected] to speak with staff.