Category
Standard
Type
Standard
Version
2
Access
Open
Status
Active
Created
2019
This document sets out the minimum requirements for best-practice use of human papillomavirus (HPV) nucleic acid testing as the primary screening method for cervical screening, with reflect liquid-based cytology in cases of positive oncogenic HPV types. Testing of self-collected specimens of symptomatic women and in the post-treatment setting has also been considered.
Main sections:
- Personnel
- Facilities
- Specimens
- Equipment
- Quality assessment
- Reporting
- Program assurance measures
- Guidance on investigating HPV detection rates (informative)
- Achieving the program assurance measures and standards for PBC (informative)
- Information required to be provided to the National Cervical Screening Register (informative)
- Program assurance measures worksheets (normative)
Main sections:
- Personnel
- Facilities
- Specimens
- Equipment
- Quality assessment
- Reporting
- Program assurance measures
- Guidance on investigating HPV detection rates (informative)
- Achieving the program assurance measures and standards for PBC (informative)
- Information required to be provided to the National Cervical Screening Register (informative)
- Program assurance measures worksheets (normative)
Access Requirements for laboratories reporting tests for the National Cervical Screening Program
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