New versions of the CathPCI Registry, Chest Pain – MI Registry and IMPACT Registry were recently released, delivering enhancements designed to help participants capture more meaningful data with greater efficiency. The new versions include streamlined workflows and logic-driven data collection, along with expanded procedural capabilities, refined reporting and guideline-aligned updates. Taken together, these enhancements are part of NCDR’s strategic work to reduce the data effort, empower care teams with actionable insights, strengthen collaboration across the continuum of cardiovascular care and support better patient outcomes. Learn more.