Under the FDA's risk-based CAPA requirements, a documented system is required for discovering the root cause of system failures, process exceptions and non-conformances. Your root cause analysis should identify why things go wrong and make sure they don't happen again.

In a new BioWorld Today and Medical Device Daily audio conference, GMP and human performance expert Vivian Bringslimark shares her expertise gained through hundreds of failure investigations. Ms. Bringslimark delves into what should be in your RCA team and common errors you could encounter. She guides you through a tool kit of proven methods of root cause analysis.

"Root Cause Analysis: Tools for Finding True Root Cause" is just $349 per listening site. Scheduled for December 17th, from 1-2:30 p.m., it includes presentation handouts and a Q&A session with the speaker. A conference CD (MP3 format) is also available. Please call 800-688-2421 or 404-262-5474 and mention conference code T08526.