Here's a look at some of the top regulatory stories for medical device companies this week: US FDA scrutinizing 3-D printing for medical devices; New FDA information on UDI rule exceptions available; FDA and Pan American Partners work to strengthen regulatory systems; FzioMed's FDA dispute panel delayed for new data submission; FDA, ONC and FCC encourage stakeholder engagement on proposed health IT strategy and framework.
US FDA scrutinizing 3-D printing for medical devices
May 30, 2014 by MassDevice
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