jmandel / interop-2019-nprms

jmandel/interop-2019-nprms Issues

Should USCDI v1 incldue more than 8 note types?
Updated 5 years ago1
Does immediate result release via APIs conflict with the "preventing harm" information blocking exclusion?
Updated 5 years ago
Add Encounter to ARCH?
Updated 5 years ago
Should "EHI export" be limited to patients/representatives?
Updated 5 years ago1
For CQM Reporting, which QRDA versions should be required (if any)?
Updated 5 years ago
Should Medication Allergy requirements be generalized to Substance Reactions?
Updated 5 years ago
Should the CDA R2 Templates for Unique Device Identification be required?
Updated 5 years ago
Is "author, author's timestamp, and author's org" the right scope for Provenance?
Updated 5 years ago
Should USCDI update to the latest version of each vocabulary?
Updated 5 years ago
How should 2015 certification critera interact with FDA Software Precertification Program?
Updated 5 years ago
Is the scope of deregulation appropriate?
Updated 5 years ago
For EHI, does "produces and electronically manages" correctly convey "entire database"?
Updated 5 years ago
Criteria to support health of children / pediatrics
Updated 5 years ago