North Texas Biomedical Association


 

  

 

Leading Practices on Compliance Series: Quality Audits

  • 12 Jan 2012
  • 10:00 AM - 11:00 AM
  • Internet

The third webinar in the series, “Quality Audits,” addresses one of the most important sections of the Quality System Regulation (21 CFR, Part 820.22).  This section requires medical device manufacturers to “establish procedures for quality audits and conduct such audits to assure that the quality system is in compliance with the established quality system requirements and to determine the effectiveness of the quality system.” 

SPEAKER

  • John Gagliardi, President,
    MidWest Process Innovation, LLC

 

 


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