CFR 42(PTS430-END) : OCT 2010
Superseded
Superseded
View Superseded by
PUBLIC HEALTH - HEALTH CARE FINANCING ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Published date
01-12-2013
Publisher
Superseded date
10-01-2011
Superseded by
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| DevelopmentNote |
Renumbered as CFR 42(PTS430-481) & CFR 42(PTS482-END). (02/2012)
|
| DocumentType |
Standard
|
| PublisherName |
Code of Federal Regulations
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| Status |
Superseded
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| SupersededBy |
| CLSI AUTO10 P : 1ED 2006 | AUTOVERIFICATION OF CLINICAL LABORATORY TEST RESULTS |
| ISO/TR 18112:2006 | Clinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devices for professional use — Summary of regulatory requirements for information supplied by the manufacturer |
| CLSI MM14 A : 1ED 2005 | PROFICIENCY TESTING (EXTERNAL QUALITY ASSESSMENT) FOR MOLECULAR METHODS |
| ASTM E 2091 : 2017 : REDLINE | Standard Guide for Use of Activity and Use Limitations, Including Institutional and Engineering Controls |
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