WebSep 24, 2014 · The issue was controversial-and important-enough to warrant inclusion in the Food and Drug Administration Safety and Innovation Act (FDASIA) of 2012, Section 617 of which clarified the definition of "Custom Devices" to provide for more leeway for the devices. FDASIA also called upon FDA to issue final guidance to clarify requirements by … Web22 hours ago · This time, join us on June 6th for ADDITIV Medical World, a half-day virtual event dedicated to bringing together the 3D printing and medical sectors. Along with ADDITIV Medical World’s sponsor, Prodways, as well as our partners SPE, SPE Additive Manufacturing, AdditiveManufacturing.com, ASME and AMGTA, we will be welcoming an …
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