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Requirements for validation of self-collected vaginal swabs for use in the National Cervical Screening Program (First Edition 2019)

This document was published by the National Pathology Accreditation Advisory Council (NPAAC) whilst under the governance of the Department of Health and Aged Care. From 1 July 2021, the Australian Commission on Safety and Quality in Health Care (the Commission) assumed responsibility for coordinating the National Pathology Accreditation (NPA) Scheme and supporting the development of the pathology accreditation standards.

Requirements for validation of self-collected vaginal swabs for use in the National Cervical Screening Program (First Edition 2019) is currently in use.

The Commission is undergoing a review process for each of the pathology standards. To remain up to date on upcoming consultations and to provide input, please visit the pathology accreditation standards and sign up now for ongoing updates.

For enquiries about the NPA Scheme or the resources, email pathology@safetyandquality.gov.au.

The Requirements Validation of Self-Collected Vaginal Swabs for Use in the National Cervical Screening Program (First Edition 2019) set out the minimum requirements that an Applicant laboratory must meet in order to offer testing of self-collected vaginal swabs for human papillomavirus as part of the National Cervical Screening Program as an in vitro diagnostic medical device.

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Requirements for validation of self-collected vaginal swabs for use in the National Cervical Screening Program (First Edition 2019)

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Publication year
2022
Resource type
Publication, report or update
Topics
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