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Lora Keena to address Root Cause Package Failure Analysis at MD&M Minneapolis, October 2008
Grand Rapids, Michigan, USA...Lora Keena, Oliver Medical director of QA/RA, has been invited to address the 2008 Medical Design & Manufacturing (MD&M) Minneapolis conference in Minneapolis. Keena's previous presentations were well received at MD&M West and MD&M East, prompting conference organizers to invite her to speak again at MD&M Minneapolis.
Keena will speak on the topic "Root Cause Package Failure Analysis" during the medical packaging conference session (#102) on October 21. The presentation will offer an overview of problem solving techniques and provide audience members with a guide to analyzing package failure, including a discussion of fishbone analysis and 'five-why' root cause analysis. Keena will also cover many possible causes of seal failure, providing case studies and several specific examples of seal defects. Audience members will have a chance to ask questions after the presentation.
Lora Keena is Oliver Medical's director of QA/RA and is responsible for initial FDA and ISO registration, inspection, and compliance for US and European facilities. Lora's areas of expertise include international auditing; quality systems; and suppliers, product, and process validation. Lora was previously director of QA/RA at LMI Medical, which was subsequently purchased by Tyco.
Oliver Medical's technical director, Randy Troutman, will chair the medical packaging conference session.
For more information, contact:
Jeff Murak
vice president of marketing & sales
616.456.7711 x7476
jmurak@olivermedical.com
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