Quality System Regulations for Laboratory Developed Tests: A Practical Guide for the Laboratory
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.
This document is available in electronic format only.
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Date of Publication: January 22, 2015
Order Code PDF: QSRLDTE
ISBN Number: 1-56238-991-2
Order Code Print: print not available