The Food and Drug Administration (FDA) has updated the information in its Frequently Asked Questions (FAQs) regarding diagnostic devices for COVID-19, including 3D printed swabs. The Administration ultimately intends to decline reviews of emergency use authorization (EUA) requests when it comes to laboratory developed tests (LDTs). The announcement comes following a release by the US […]
from 3D Printing Industry https://bit.ly/2SHRfMV