Common - Clinical Document v1.2.1

FAQs for EP-1094:2011 Common - Clinical Document v1.0.2, EP-1457:2013 Common - Clinical Document v1.1, EP-1477:2013 Common - Clinical Document v1.1.1, EP-1589:2014 Common - Clinical Document v1.1.2, EP-1754:2014 Common - Clinical Document v1.1.3, EP-1815:2014 Common - Clinical Document v1.2, EP-1962:2014 Common - Clinical Document v1.2.1, EP-2024:2015 Common - Clinical Document v1.2.2, EP-1818:2015 Common - Clinical Document v1.3, EP-2085:2015 Common - Clinical Document v1.3.1, EP-2198:2015 Common - Clinical Document v1.4, EP-2231:2016 Common - Clinical Document v1.4.1, EP-2241:2016 Common - Clinical Document v1.4.2

The guidance contained in this document has been superseded and should no longer be used for implementations of clinical documents specifications.This document describes requirements for how to represent MIMS codes in CDA documents.

This specification defines a clinical package as a logical model of the data it contains. This model can be profiled to create data models for specific clinical data.

What is the appropriate use of date and date-time values in clinical documents?

FAQ

The FAQs are guidance material for implementation. They should be used for clarification purposes and to support existing documentation.

The FAQ Patient Medications has been archived and is no longer included in this end product release. Its contents have been superseded by updates to the latest versions of the CDA Implementation Guides for Event Summary and Specialist Letter document types.

Supplementary Notes for Implementers Relating to Clinical Document Presentation v1.0

Conformance test specification for CDA rendering.

This document summarises the common requirements for producers and consumers of clinical documents.

This release introduces an updated version of the Common – Clinical Documents - PCEHR Usability Recommendations and provides an update of the Template Package Directory.