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FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies
This Webinar is over| Date | Oct 2, 2018 |
| Time | 03:00 PM EDT |
| Cost | $200.00 |
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Online
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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 :
Who Should Attend:
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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