CLSI I/LA6 A : 1ED 97
Withdrawn
Withdrawn
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
01-12-2013
Publisher
Withdrawn date
07-23-2013
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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Withdrawn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 |
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