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2019 - Getting to Know FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies
Date2019-08-27
Deadline2019-08-27
VenueOnline Event, USA - United States 
KeywordsFDA auditing practices; FDA warning letters 483; FDA enforcement actions
Topics/Call fo Papers
Changes in FDA audit approaches
Most common cited GMP drug deficiencies for 2017-2018
Increase in FDA enforcement actions
How best to address FDA 483 observations when received
Areas of focus
Most common cited GMP drug deficiencies for 2017-2018
Increase in FDA enforcement actions
How best to address FDA 483 observations when received
Areas of focus
Other CFPs
Last modified: 2019-07-04 20:25:59