Date :
Place : United States, Fremont
Contact Person:Event Manager
Description:
This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. We will discuss the myths, challenges, and best practices for this critical process. We'll also cover the essentials of doing a failure investigation.Deadline for abstracts/proposals : 8th January 2019
Organized By :Traininng.com LLC
Keynote Speakers : Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities. While at GE, J&J, and Medtronic, Susanne worked in various world-wide roles including Executive Business Consultant, WW Director of Quality Engineering and, Design Quality, and Director of Corporate Compl
Conference Highlights :Build the right team Develop a problem statement Failure Investigation Data Collection Analysis Tools and Techniques How to Verify your Results Real Lessons Learned Do's and Don'ts of CAPA Best Practices Inspection Readiness
Venue :Fremont, CA, USA
Check the event website for more details.