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Bridging the Gap, RSSearch™ Patient Registry Quarterly Newsletter
To view and/or print a copy of the newsletter please use the following links:
RSSearch™ Patient Registry Videos
Introduction to RSSearch™
- This 9 minute video provides an overview of data fields collected in the RSSearch Patient Registry.
Bridging the Gap: the RSSearch Patient Registry
- This 15 minute video captures Joanne Davis, PhD giving a brief history of the registry, sharing some of the reporting features as well as outcomes data for liver and brain mets and NSCLC.
About the RSSearch™ Patient Registry
The RSSearch™ Patient Registry is an international multi-platform research and data sharing registry aimed at generating peer reviewed publications and increasing collaboration among the diverse clinical specialties, hospitals and industries participating in SRS and SBRT. Participation in RSSearch is aimed at using data to improve the quality of care and medical decision making, access to novel treatments and approaches for patients, and furthering the development and science of SRS/SBRT treatment. Eventually, Clinical and quality guidelines based on evidence-based approaches will emerge from the registry. To participate, IRB approval is required.
Benefits of participating in RSSearch include:
Secure web-based patient management registry designed to serve an entire SRS/SBRT patient population
Ability to better track patient follow-up
Allows secure and real-time access to your patient information
Generate a wide variety of standard and customized reports
Easy access to your treatment and outcomes data for publication and presentation
Access to aggregate data upon application (
for Request for Aggregate Data Form)
HIPAA and EU compliant
to view the flyer,
watch the video demo
or for more information, please email Nalani Brown at
Requests for Aggregate Data
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