FDA-CLINICAL LABORAT › Guidance for Industry and FDA Staff: Recommendations for Clinical Laboratory Improvement Amendments of 1988 (CLIA) Waiver Applications for Manufacturers of In Vitro Diagnostic Devices

FDA-CLINICAL LABORAT - 2008 EDITION - CURRENT



Guidance for Industry and FDA Staff: Recommendations for Clinical Laboratory Improvement Amendments of 1988 (CLIA) Waiver Applications for Manufacturers of In Vitro Diagnostic Devices


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Document Number

FDA-CLINICAL LABORAT

Revision Level

2008 EDITION

Status

Current

Publication Date

Jan. 30, 2008

Page Count

45 pages