Part 4 of 4: Why better planning for surgical growth, operational performance, and patient safety requires sterile processing expertise early in the decision-making process.
|Articles|July 19, 2011
AAMI Announces Medical Devices Summit in October
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The Association for the Advancement of Medical Instrumentation (AAMI) and the Food and Drug Administration (FDA) invite members of the medical community to participate in a special summit focusing on critical issues related to the reprocessing of medical devices, Oct. 1112, 2011, at the FDA headquarters in Silver Spring, Md.
Building from the FDA's public meeting of June 8-9, 2011, leaders from industry, regulatory bodies, and associations; clinicians from healthcare institutions; subject experts; patient safety officers; researchers; and others will gather to identify, discuss, and formulate strategic initiatives and priorities to improve the safe reprocessing of reusable medical devices.
Pre-registration is required. You must have written confirmation from AAMI to participate in the summit. To register,
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Understanding current water quality is a starting point for ST108 implementation. John Kimsey, vice president of processing optimization and customer success for STERIS, spoke about his HSPA presentation on assessing readiness, distinguishing system qualification from routine testing, and understanding where water samples should be collected.
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