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Clinical and Laboratory Standards Institute , 09/01/2024
Publisher: CLSI
File Format: PDF
$90.00$180.00
This practical guide, compiled with the help of experts from the in vitro diagnostics industry, is intended for the laboratory that is creating laboratory developed tests that may be subject to the US Food and Drug Administration (FDA) regulations, specifically the Quality System Regulation (QSReg), 21 CFR Part 820.
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