The Most Serious FDA 483s - How to Avoid Them 2019

  • 12 Mar 2019
  • Webinar

Description

The Most Serious FDA 483s - How to Avoid Them 2019 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 2019 brings together:

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

Past Events

Important

Please, check "The Most Serious FDA 483s - How to Avoid Them" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Pharma
Science: Life Sciences & Biology

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