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Seminar on How FDA Trains Its Investigators to Review Sub-Systems for State of C

The Seminar will provide all details relevant to Pre and Post-Inspectional activities, tactics, strategies

We will address FDA enforcement stats in this space with some regularity, trying to discern patterns and trends as related to current state vs. future state. We will address the critical approach necessary to develop a quality remediation plan for inspectional observations (e.g., FDA Form 483/Warning Letter) submitted by FDA. 


17 Mar 2016 @ 09:00 am

18 Mar 2016 @ 06:00 pm

Duration: 1 days, 9 hours


Trump Taj Mahal

1000 N Virginia Ave

United States



Organised by

GlobalCompliancePanel (deactivated)

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