Over the past year numerous medical device companies have been issued warning letters for non-compliant quality system internal audits. Violations include the lack of auditing procedures to insufficient audit frequency, failure to re-audit, and simple documentation oversights.

In a new Medical Device Daily audio conference, speaker Susan Reilly, a recognized expert in the medical device industry, will demonstrate how to organize and coordinate internal audits, from initial planning to team selection, execution and documentation, and analysis and planning for the next audit.

"Quality System Audits: Lessons Learned in Medical Device Risk Management" is just $349 per listening site. Scheduled for June 17th, from 1-2:30 p.m., it includes presentation handouts and a half-hour Q&A session with the speaker. A conference CD (MP3 format) is also available. For more information or to register, call 800-688-2421 or 404-262-5474. Please mention conference code T08498.