Introduction
The following steps will assist Clinical Information System (CIS) software developers with a direct Prescription Delivery Service (PDS), declare software conformance with Australia Digital Health Agency (the Agency’s) Electronic Prescribing technical framework. A direct PDS generally provides the capability to prescribe and dispense, without the requirement to dispense from a community pharmacy, commonly used in hospitals.
If your product uses different model, explore other options available here:
Pre-requisites
- None
Step 1: Develop Your Product
Review the latest version of the Electronic Prescribing Conformance Profile within the Technical Framework documentation available here:
Identify the applicable requirements/conformance points that apply to your product. Each requirement identifies if it is applicable to a Direct PDS model. Look for a "yes" under the "Direct PDS" column to see if it applies. If it says "no," that requirement does not apply.
Also consider the requirements that apply to direct medication chart PDS. The applicable conformance requirements are marked with “yes” in the “Med charts Direct PDS” column.
Conformance Test Specifications and test data are available to assist your development and testing here:
Commence developing your product.
Note:
Please ensure you check the specific requirements of the states and/or territories in which you intend to release your product. Some states and territories have established approval criteria software developers must meet prior to deployment. Details available here:
Step 2: Conduct Internal Testing
Conduct a self assessment against the applicable requirements/conformance points and your own internal testing.
Step 3: Complete the Conformance Test Specification
Complete the Electronic Prescribing Conformance Test Specification (CTS) and submit to the Agency.
Please ensure the CTS for your product, completed in full, with:
- the relevant test outcomes (pass, fail, N/A) recorded against each test case
- a corresponding reason documented for any test marked as N/A
- completed Test Summary Report (TSR) worksheet
- relevant evidence for each test outcome including screenshots, recordings, documentation or other.
Step 4: Conduct Conformance Assessment
The Agency will conduct your Conformance Assessment observation session.
The purpose of the observed Conformance Assessment is to verify and confirm the results recorded in your submitted CTS and validate any further information requested by the Agency.
You will be informed by the Agency if you are ready to undergo observation and will schedule the session at a mutually agreeable time.
During and following your observed Conformance Assessment, the Agency may request further evidence for specific test cases to ensure the record of the test is full and accurate.
Step 5: Declare Conformance
After successfully completing the observed Conformance Assessment, fill out the Electronic Prescribing Conformance Vendor Declaration Form. Email your form to help@digitalhealth.gov.au. Please ensure that:
Complete the after the observed conformance assessment is successfully completed.
- you have completed all relevant information, such as inclusion of companion software details in section 1.3. Companion software may include PDS adaptor(s), workflow engine(s), mobile gateway(s), etc.
- the information in the form matches the information in the Test Summary Report tab in the final CTS.
Note: The Conformance ID requested in the form is a string of no more than 36 printable characters containing a text string representing the product name, a single character delimiter (“|”) and an alphanumeric string representing the software product version. As the Conformance ID may help with issue identification and is used to manage participation, it is strongly advised that you declare accurate version information. It is, however, recognised that some software products update version information regularly and in response to changes that do not impact electronic prescribing functionality. For this reason, software vendors may ascertain for themselves the granularity of version information declared in the Conformance ID and the occasions at which it is declared.
If the Agency identifies any issues in your submission, you will be informed directly. Upon successful processing, you will be notified by the Agency directly and your product will be added to the register of conformance. This register is communicated by the Agency to Services Australia, State and Territory Health departments and PDS providers for operational purposes.
Step 6: Deploy Updated Product
Once you have received a notification that your product has been included on the list of conformant products you may commence deploying electronic prescribing functionality into production and conduct associated training to your end users.
Conclusion
You are now ready to achieve product conformance with the Agency's Electronic Prescribing Technical Framework for your Direct PDS CIS products. If you need any further assistance please contact help@digitalhealth.gov.au.