Archived

This document describes the development approach used by the National Clinical Terminology and Information Service (NCTIS) in creating reference sets for use by the AMT community of practice. The reference sets have been developed by the NCTIS within the Agency.

  Clinical Document Library (Java) to support the PCEHR R5 documents Pathology Report and Diagnostic Imaging Report. This product component was previously called CDA Document Library - Java Sample Code. The name has changed but the content has not changed.   This document mentions the NPDR. Please note: the National Prescription…

Conformance test specification for clinical documents

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

The FAQ Patient Medications has been archived and is no longer included in this end product release. Its contents have been superseded by updates to the latest versions of the CDA Implementation Guides for Event Summary and Specialist Letter document types.

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

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

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

The guidance contained in this document has been superseded and should no longer be used for implementations of clinical documents specifications.

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 are the nullable fields in clinical documents conformant to the CDA implementation guides

The Common - Continuity of Care end product has been archived. The remaining three components have been moved to Common - Clinical Documents. These are: FAQ Nullable Fields Guidance v1.1 FAQ Global Statements None Known v1.1 FAQ Undifferentiated Pathology and Radiology Results v1.3 Future updates to the FAQs will be published in Common - Clinical Document.