A common application for micro fluidics can be found in medical devices where the advantages of small volume measuring equipment can be exploited for In Vitro Diagnostics. This chapter focuses on the US and the EU regulations, explaining the broad landscape and regulatory pathways of each market. © Springer Science+Business Media, LLC 2013.
CITATION STYLE
Day, J. (2013). Introduction to in vitro diagnostic device regulatory requirements. Methods in Molecular Biology. Humana Press Inc. https://doi.org/10.1007/978-1-62703-134-9_7
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