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
