Why “We Support HL7” Is Not Enough: A Buyer’s Field Guide
A practical guide for Arizona organizations evaluating interoperability claims, with the specific qu...
A practical guide for Arizona organizations evaluating interoperability claims, with the specific qu...
The U.S. Core Data for Interoperability expands on a yearly rhythm, and the FHIR US Core guide track...
Supply-chain interoperability rests on identifying products, locations, and shipments unambiguously....
An explainer on the messaging, directories, and identity controls that move an electronic prescripti...
GS1’s GTIN is one of the identifier systems FDA accepts for UDI. We explain how supply-chain identif...
RPM is often framed as a billing or device topic. We examine the data-standards and integration laye...
Tracing the path device data travels — from a bedside pump to a structured, coded entry in the medic...
A device identifier is only useful if it is captured where care happens. We examine the workflow, do...
Health information exchange is moving from trading whole documents toward querying discrete data ele...
HL7 version 2 still carries most real-time clinical messaging. A guided walk through the segments of...
A practical explainer separating FHIR, US Core, and USCDI — three layers providers conflate — and wh...
The FDA’s Unique Device Identification rule finished its long, risk-tiered rollout. We summarize whe...
HL7’s FHIR Release 4 was the first version of the standard to carry normative content, giving Arizon...