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 Testing Method

For each proficiency test a panel of samples is sent to each participating laboratory for testing.  The panel is comprised of six samples with at least one negative, one low positive and one high positive sample if available to reflect a range of results likely to be found in routine diagnostic testing.  Laboratories are encouraged to treat the panel as diagnostic specimens and include them within the routine testing schedule. 

 The laboratory is given approximately 4 weeks to test and report results.  ANQAP collate the results and prepare a report summarising the results of all laboratories. The ANQAP report includes statistical analysis where appropriate, and a classification of the results.  Results that fall within an acceptable variation range are classified as satisfactory.  If the results demonstrate variation, the laboratory is given the opportunity to retest a fresh vial of the same sample.  Following retesting the result is classified as either retest satisfactory, retest demonstrating minor variation or retest unacceptable.  Laboratories receiving an unacceptable classification are encouraged to take corrective action.

 The design of the program meets the requirements of ILAC G13:2007 Guidelines for the Requirements for the Competence of Providers of Proficiency Testing Schemes.