Collecting standardized data to improve clinical care
Clinical registries are organized systems that store standardized data on a specific population defined by a disease, condition or procedure. Information from clinical data registries can be used to evaluate specific outcomes and compare the effectiveness of different treatments. Furthermore, they are used to improve the quality of care and patient safety.
The Clinical Research and Registries Division strongly encourages registry endeavors for the purposes of advancing scientific knowledge and developing innovative therapies that lead to improved patient care in IR. Previous registry stakeholders include government agencies, industry manufacturers and other professional societies.
SIR Foundation is currently supporting multiple registries. To learn more about these registries, please click the box below.Learn more
To learn more about the completed registries that SIR Foundation has supported, please click the link below.Learn more
Are you interested in starting a registry? If so, learn about how to submit an idea to SIR Foundation through our letter of intent (LOI) process.Learn more