Kidney Research Network

KRN welcomes and encourages investigators within and external to the network to use registry data for their own research. Research proposals are reviewed and prioritized by the Registry Steering Committee.  Data domains available include: laboratories, medications, diagnosis, procedures, biopsy information, vitals, demographics, and transplant data.

 

Read more about the KRN registry data and how it may be used here.

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Download the KRN ancillary study application and following instructions within for submission. 

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Ancillary studies are subject to the following KRN policies governing registry data:

• KRN Policy on Data Use

• KRN Policy on Publication