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Medical Laboratory Quality Systems and Accreditation ” Reporting results” Please read the file before doing anthing.
Please answer these questions.
1. How are report formats determined in your laboratory and who provides input into the decision on the final format?
2. Who is able to validate and authorise the release of results from your laboratory? What referral policy does your laboratory have in place for results to go to registars/pathologists for review prior to release of results from the laboratory?
3. What are the implications of autovalidation, autoauthorisation and decision support systems for the interpretation and release of results from the laboratory.
4. The standard indicates that upon request, information on detection limits and uncertainty of measurement should be provided. If the laboratory has this information why isn’t it included in the report as a matter of routine? Of what value is this information if it is retained by the laboratory and not used to better inform clinicians of the significance of the results they have been given?
5. How do you determine uncertainty of measurement for a range of the analytes tested in your laboratory?
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