FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies

MessageThis Webinar is over
Date Oct 2, 2018
Time 03:00 PM EDT
Cost $200.00
This webinar will look at changes in FDA’s approach to audits and the current method used to determine audit frequencies by using a system of risk assessments.

Areas Covered in the Session :
  • Changes in FDA audit approaches
  • Areas of focus during audits
  • Most commonly cited drug GMP deficiencies for 2012-2013
  • Increase in FDA enforcement actions
  • Interactive Q&A Session

Who Should Attend:
  • Quality Assurance Teams
  • Quality Control Teams
  • Manufacturing Teams
  • Validation Teams
  • Production Teams
  • Regulatory Compliance Teams


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