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The Most Serious FDA 483s - How to Avoid Them 2019
12 Mar 2019
Webinar
Home
The Most Serious FDA 483s - How to Avoid Them 2019
Description
Topics
The "Whys"
Recent Most Serious FDA 483s
Avoid complacency from past "good" FDA audits
Root Causes
Maximize scarce resources
Shifting focus
Maintain "the edge" -- fight "entropy"
The "risk-based" phased approach
Who should Attend
Regulatory Affairs
Senior management
Production
Quality Assurance
Engineering
Past Events
The Most Serious FDA 483s - How to Avoid Them 2019 - 12 Mar 2019, Webinar
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Important
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