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

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