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SSBA – Form – Non-registered facility report for temporary handling and disposal of an SSBA
Use this form to report the temporary handling and disposal of a known SSBA (previously confirmed in another facility). Temporary handlings must be for 7 working days or less. -
SSBA – Form – Change the purpose for handling an SSBA
Use this form to report changes to the purpose for handling a registered security sensitive biological agent (SSBA), including ceasing a purpose and adding a purpose. -
SSBA – Form – Start to handle a new SSBA
Registered facilities must use this form to report when they handle a new security sensitive biological agent (SSBA) that they are not currently registered for. -
SSBA – Form – Destruction of SSBA
Use this form to report when all of an SSBA is destroyed or the remaining quantity falls below the reportable quantity for a toxin. You can also use this form to de-register. Non-registered facilities that have already provided this information in the relevant form do not have to fill in this form. -
SSBA – Form – Incident report
Registered facilities should use this form to report an incident that is defined as a reportable event, whether it occurs intentionally or by accident. -
SSBA – Form – Application for extension
Use this form to apply for an extension when you are required to handle an SSBA for longer than 2 business days. Please note that this is not required when waiting for the results of confirmatory testing. -
SSBA – Form – Transfer out an SSBA
Use this form to report the transfer of security sensitive biological agents (SSBAs) out of your facility. You can also use this form to apply to de-register. -
SSBA – Form – Change of responsible officer details
Use this form to report changes to the Responsible or Deputy Responsible Officer or their contact details. -
SSBA – Form – Change to entity and facility details
Use this form to report changes to your entity or facility details. -
SSBA – Form – Removal of Salmonella Typhi and Vibrio cholerae
Use this form for the removal of Salmonella Typhi and Vibrio cholerae. -
SSBA – Form – Registered facility report for suspected SSBAs and confirmatory results
Facilities registered to handle security sensitive biological agents (SSBAs) should use this form to report specific information about SSBAs. -
SSBA – Form – Registered facility report for temporary handling and disposal of an SSBA
Use this form to report the temporary handling and disposal of a known SSBA (previously confirmed in another facility) that you are not registered for. Temporary handlings must be for 7 working days or less. -
SSBA – Form – Transfers between facilities of the same entity
Registered facilities must use this form when transferring security sensitive biological agents (SSBAs) to another facility within the same entity. -
SSBA – Form – Registration of a linked storage unit
Use this form if you are already a registered facility and want to register a linked storage unit to store Tier 2 SSBAs under Part 4A.5 of the SSBA Standards. To register a new facility, use the Initial Registration form. -
SSBA – Form – Transfer in an SSBA
Use this form to report the transfer of security sensitive biological agents (SSBAs) into your facility. You must report as soon as possible and within 2 business days of the transfer occuring. -
Q fever – Surveillance case definition
This document contains the surveillance case definition for Q fever, which is nationally notifiable within Australia. State and territory health departments use this definition to decide whether to notify us of a case. -
Tularaemia – Surveillance case definition
This document contains the surveillance case definition for tularaemia, which is nationally notifiable within Australia. State and territory health departments use this definition to decide whether to notify us of a case. -
Modified Monash Model – fact sheet
Information about the Modified Monash Model geographical classification. -
Approved Private Emergency Department Program guidelines
These guidelines provide the background, principles, eligibility criteria and operational procedures of the program for participating hospitals. -
BreastScreen Australia – Quality matters bulletins
These bulletins report on current National Quality Management Committee (NQMC) news, events and opportunities for BreastScreen Australia Services. -
National Vaccine Storage Guidelines ‘Strive for 5’, Appendix 9 – Checklist for Managing a Power Failure
Use this checklist for emergency storage of vaccines including power or refrigerator failure. -
Quality of Information and Guidance Industry Working Group Terms of Reference
This document sets out the roles, function, membership and operating guidelines of the Quality of Information and Guidance Industry Working Group. -
National Vaccine Storage Guidelines ‘Strive for 5’, Appendix 8 - Checklist: Mobile and emergency storage
National Vaccine Storage Guidelines ‘Strive for 5’, Appendix 8 includes a checklist and temperature chart for mobile or outreach immunisation clinics, or emergency storage of vaccines. -
National Vaccine Storage Guidelines ‘Strive for 5’, Appendix 2 - Vaccine Storage Self Audit
‘Strive for 5’ National Vaccine Storage Guidelines vaccine storage self-audit checklist. -
National Aged Care Mandatory Quality Indicator Program Manual 2.0 – Part A
This version of the manual was in effect from 1 July 2021 to 31 March 2023.