The Association for the Advancement of Medical Instrumentation (AAMI) and the Food & Drug Administration (FDA) kick-off their 2-day medical device reprocessing summit today in Silver Spring, MD at the FDA’s White Oak campus. Building from the FDA’s public meeting of June 8-9, 2011, leaders from industry, regulatory bodies, and associations; clinicians from health institutions; subject experts, patient safety officers; researchers; and others will gather to identify, discuss, and formulate strategic initiatives an priorities to improve the safe reprocessing of reusable medical devices.
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Be sure to check back regularly on AMDR’s website, Twitter, and Facebook for updates from the event.