CLSI I/LA18-A2

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This guideline outlines specimen requirements; performance criteria; algorithms for the potential use of sequential or duplicate testing; recommendations for intermethod comparisons of immunological test kits for detecting infectious diseases; and specifications for development of reference materials.This document is no longer being reviewed as part of the CLSI consensus process. However, because of its usefulness to a limited segment of the healthcare community, CLSI is continuing to make the document available for its informational content.

This document is available in electronic format only.

Product Details

Edition:

2nd

Published:

09/20/2001

ISBN(s):

1562384457

Number of Pages:

46

File Size:

1 file , 1.8 MB