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.

Click Here for More Information

Be sure to check back regularly on AMDR’s websiteTwitter, and Facebook for updates from the event.