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Clinical and Laboratory Standards Institute, 09/20/2002
Publisher: CLSI
File Format: PDF
$120.00$240.61
Published:20/09/2002
Pages:56
CLSI EP09-A2 addresses procedures for determining the bias between two clinical methods or devices, and for the design of a method comparison experiment using split patient samples and data analysis.
The U.S. Food and Drug Administration (FDA) has evaluated and recognized this approved-level consensus guidleine for use in satisfying a regulatory requirement.
Procedure for the Collection of Diagnostic Blood Specimens by Venipuncture; Approved Standard, Fifth Edition, H03A5E
$139.00 $279.21
IT Security of In Vitro Diagnostic Instruments and Software Systems; Proposed Standard, AUTO11AE
$119.00 $239.13
Autoverification of Clinical Laboratory Test Results; Approved Guideline, AUTO10AE
$90.00 $180.00
Point-of-Care In Vitro Diagnostic (IVD) Testing; Approved Guideline, POCT4A2E
$118.00 $237.30
