AAMI Offers Ethylene Oxide Sterilization for Medical Devices Workshop

<p>The Association for the Advancement of Medical Instrumentation (AAMI) announces that the Industrial Ethylene Oxide Sterilization for Medical Devices Workshop, a three-day, highly interactive advanced workshop, will be held October 4-6, 2010 at the Westin Peachtree Plaza in Atlanta.</p>

The Association for the Advancement of Medical Instrumentation (AAMI) announces that the Industrial Ethylene Oxide Sterilization for Medical Devices Workshop, a three-day, highly interactive advanced workshop, will be held October 4-6, 2010 at the Westin Peachtree Plaza in Atlanta. The workshop assumes that participants are experienced in working with an established ethylene oxide sterilization process, but are now challenged with ensuring the continued effectiveness and assessing change for the product or process. The program combines classroom lecture with real-life scenarios to illustrate concepts and situational analyses that provide participants with the opportunity to apply what they learn to actual sterilization scenarios.

Upon completion of this workshop, participants will be able to improve development and routine turn-around time; make changes to product, equipment, process and sterilizer location; determine if validation or requalification is necessary; troubleshoot cycle anomalies; and optimize the the ethylene oxide sterilization process.

This workshop is designed for professionals that have responsibility for making decisions related to the ethylene oxide sterilization process such as introduction of new/modified products, sterilization process improvements, failure investigation, requalification, and validation. AAMI recommends this workshop for those who are experienced in working with an established ethylene oxide sterilization process and not professionals that are new to ethylene oxide sterilization.

Workshop faculty are drawn from an experienced group of quality systems professionals. All faculty have completed an instructor training program to ensure consistency and quality from session to session. The mix of industry leaders, consultants, and FDA personnel helps to ensure a balanced presentation of the requirements and paths to compliance.

For fees, more details and to register, CLICK HERE.

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