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Lora Keena to address Root Cause Package Failure Analysis at MD&M West, January, 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) West conference in Anaheim. Keena will speak on the topic "Root Cause Package Failure Analysis" during the medical packaging conference session on January 28.
During her presentation, Keena will provide audience members with a guide to analyzing package failure, including a discussion of fishbone analysis and 'five why' root cause analysis. She will also cover many possible causes of seal failure in detail, providing case studies and numerous specific examples of seal defects.
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 supplier, 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
director of marketing & sales
616.456.7711 x7476
jmurak@olivermedical.com
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