The Most Serious FDA 483s - How to Avoid Them

The Most Serious FDA 483s - How to Avoid Them is a webinar that covers topics such as:

  • 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

The Most Serious FDA 483s - How to Avoid Them brings together:

  • Regulatory Affairs
  • Senior management
  • Production
  • Quality Assurance
  • Engineering

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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