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Resources for the pathology standards
The resources below support clinicians, service providers and accrediting agencies by providing guidance on the requirements for pathology laboratories to be accredited.
Notice
From 1 July 2021, the Australian Commission on Safety and Quality in Health Care (the Commission) is responsible for coordinating the National Pathology Accreditation (NPA) Scheme and managing the development of the pathology accreditation standards.
For enquiries about the NPA Scheme or the resources provided below, email pathology@safetyandquality.gov.au.
Testing for COVID-19
In response to the coronavirus diseases 2019 (COVID‑19) pandemic, the National Pathology Accreditation Advisory Council (NPAAC) has developed a number of resources relating to COVID‑19 to support the Australian healthcare system.
NPAAC has developed guidance to support the increased demand in COVID‑19 testing in various healthcare settings such as hospitals, pathology laboratories and primary healthcare services.
This guidance complements NPAAC’s existing Guidelines for point of care testing.
State and territory governments and service providers established temporary collection facilities such as drive throughs and pop‑ups to broaden specimen collection for COVID‑19 testing in the community.
In July 2020, NPAAC released guidelines to support temporary collection facilities during the COVID‑19 pandemic. The guidelines were developed to protect consumers and ensure consistency in pathology results.
Errors and corrections
Advisories
Fact sheets and FAQs
Recording – Understanding the NPAAC Requirements for supervision in the clinical governance of medical pathology laboratories seminar
Best practice guidelines
Previous editions of the standards (updated as of July 2023)
This document has been superseded by Requirements for supervision in the clinical governance of medical pathology laboratories (Seventh Edition 2023).
This document has been superseded by Requirements for the packaging and transport of pathology specimens and associated materials (Fifth Edition).
This document has been superseded by Requirements for information communication and reporting (Fifth Edition).
Genetic pathology
This document has been superseded by Requirements for medical testing for human genetic variation (Third Edition).
This document has been superseded by Requirements for medical testing for human genetic variation (Third Edition).
Haematology
This document has been superseded by Requirements for transfusion laboratory practice (Fifth Edition).
Microbiology
This document has been superseded by Requirements for laboratory testing for human immunodeficiency virus (HIV) and hepatitis C virus (HCV) (Fourth Edition).
Feedback
The Commission values your opinion. You can provide comments and feedback about this section of the Commission’s website by emailing advicecentre@safetyandquality.gov.au or phone 1800 304 056.