Common - Clinical Document v1.2.1

Specifications, guidance and associated collateral applicable to all types of clinical documents.

NOTE: The sample code previously available in this end product is now available in:

 

End products superseded by

A new version has been released for this end product

Please refer to Common - Clinical Document v1.2.2 or refer to the Release History for all releases of this End Product.

Identifier: 
EP-1962:2014
Date: 
31-12-2014
Type: 
application/zip
SHA256 Checksum: 
60ba8964ed15757b45c10d9ff6886e3e94a48735326664f46b21d30759cdeb17
Size: 
6.31 MB

Product Components

Product component
Identifier: 
NEHTA-1096:2011

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

Product component
Identifier: 
NEHTA-1097:2011

This document provides advice for implementers with respect to coding common clinical concepts in Agency CDA documents, including e-Referral, Discharge Summary, Event Summary, Shared Health Summary, and Specialist Letter.

Product component
Identifier: 
NEHTA-1165:2012

The guidance contained in this document has been superseded and should no longer be used for implementations of clinical documents specifications.

Product component
Identifier: 
NEHTA-1199:2012

This document:

Product component
Identifier: 
NEHTA-1226:2011

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.

Product component
Identifier: 
NEHTA-1229:2011

This specification defines three logical models for clinical data that consists of a single CDA XML document and related byte streams. This specification also defines a possible serialised representation for those logical models.

Product component
Identifier: 
NEHTA-1255:2012

This FAQ answers the question: What is the appropriate use of date and date-time values in clinical documents?

Product component
Identifier: 
NEHTA-1256:2012

Question: When receiving a CDA® package, how can we ensure that the content is from a trusted source?

Product component
Identifier: 
NEHTA-1270:2013

This FAQ describes an extension to these eDischarge Summary, eReferral and Specialist Letter that involves encapsulating the CDA package within an HL7 v2 MDM^T02 message (which covers the delivery of a document).

Product component
Identifier: 
NEHTA-1271:2013

A list of attachment document types specified in the CDA Rendering Specification v1.0 and those supported by the My Health Record system.

Product component
Identifier: 
NEHTA-1276:2013

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

Product component
Identifier: 
NEHTA-1275:2013

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

This FAQ answers the question: What is the proper representation of pathology test result date/time?

Product component
Identifier: 
NEHTA-1277:2013

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.

Product component
Identifier: 
NEHTA-1278:2013

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

This FAQ answers the question: How to represent patient identifiers (other than IHIs) in CDA documents?

Product component
Identifier: 
NEHTA-1328:2013

This document recommends a set of presentation guidelines for CDA® document authors. It complements the CDA® Rendering Specification and the CDA® implementation guides by describing:

Product component
Identifier: 
NEHTA-1329:2012

Conformance test specification for clinical documents

Product component
Identifier: 
NEHTA-1330:2012

Conformance test specification for CDA rendering.

Product component
Identifier: 
NEHTA-1331:2012

Conformance Test Specification for CDA Packaging

Product component
Identifier: 
NEHTA-1812:2014

This document provides conformance requirements applicable to all types of clinical documents. This includes references to other documents containing additional normative content.

Product component
Identifier: 
NEHTA-1923:2014

This document provides usability recommendations for clinical information systems and contracted service provider systems authoring or rendering information contained in clinical documents and views exchanged with the My Health Record system.
 

Product component
Identifier: 
NEHTA-1965:2014

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

Product component
Identifier: 
NEHTA-1849:2014

The Template Package Directory provides a comprehensive overview of available template packages and their current status.
 

Release history

By operation of the Public Governance, Performance and Accountability (Establishing the Australian Digital Health Agency) Rule 2016, on 1 July 2016, all the assets and liabilities of NEHTA will vest in the Australian Digital Health Agency. In this website, on and from 1 July 2016, all references to "National E-Health Transition Authority" or "NEHTA" will be deemed to be references to the Australian Digital Health Agency. PCEHR means the My Health Record, formerly the "Personally Controlled Electronic Health Record", within the meaning of the My Health Records Act 2012 (Cth), formerly called the Personally Controlled Electronic Health Records Act 2012 (Cth).

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