Common - Clinical Document v1.5.4
Products, Specifications | EP-3149:2020
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
The Common - Clinical Document end product provides developers of systems generating CDA documents with important updates of:
The Common - Clinical Document end product provides developers of systems generating CDA documents with important updates of:
Specifications, guidance and associated collateral applicable to all types of clinical documents.
The detailed specifications for all clinical documents are available
The Australian Digital Health Agency has released version 3.2 of the Clinical Package Validator.
The Agency has released updates for the following products Clinical Documents Integration Toolkit v1.8 and Health Record Overview v1.2
The Australian Digital Health Agency (the Agency) has released version 2.8 of the Clinical Package Validator. The Clinical Package Validator v2.8 now supports the execution of enhanced validation rules for clinical documents: Information Quality Rules (IQ Rules).
The Australian Digital Health Agency (the Agency) has released a new major release of its HIPS middleware product: HIPS 7.0
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).