CLSI I/LA6 A : 1ED 97
Withdrawn
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
DETECTION AND QUANTITATION OF RUBELLA IGG ANTIBODY: EVALUATION AND PERFORMANCE CRITERIA FOR MULTIPLE COMPONENT TEST PRODUCTS, SPECIMEN HANDLING, AND USE OF TEST PRODUCTS IN THE CLINICAL LABORATORY
Published date
12-01-2013
Publisher
Withdrawn date
23-07-2013
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Identifies performance specifications and criteria for products used to detect rubella antibody. Provides procedures for collecting and handling specimens submitted for rubella serological testing, evaluation and reporting results.
| DevelopmentNote |
Supersedes NCCLS I/LA6 T & NCCLS I/LA7 P (10/2000) I/LA6 A is no longer being reviewed as part of NCCLS consensus process. However, because of its usefulness to a limited segment of the healthcare community, NCCLS is continuing to make the document available for its informational content. This document is available in electronic format only. (04/2005)
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| DocumentType |
Miscellaneous Product
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| PublisherName |
Clinical Laboratory Standards Institute
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| Status |
Withdrawn
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| Supersedes |
| BS EN 13612:2002 | Performance evaluation of in vitro diagnostic medical devices |
| I.S. EN 13612:2002 | PERFORMANCE EVALUATION OF IN VITRO DIAGNOSTIC MEDICAL DEVICES |
Summarise
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