Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies 2018

  • 26 Sep 2018
  • Webinar

Description

Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies 2018 is an event dedicated to the current audit techniques used by FDA and how they have changed over the years.

Topics
  • Changes in FDA audit approaches
  • Increase in FDA enforcement actions
  • Most common cited GMP drug deficiencies for 2012-2015
  • How best to address FDA 483 observations when received
Who should Attend
  • Quality Assurance
  • Who Will Benefit:
  • Manufacturing
  • Quality Control
  • Regulatory
  • Production
  • Management
  • Laboratory Personnel
  • Equipment Vendors

Past Events

Important

Please, check "Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Finance, Innovations, Internal Audit & Compliance, Management, Operations, Procurement, Quality assurance, Risk Management
Government & Global Issues: Law & Regulations
Health & Medicine: Family medicine, Healthcare, Internal medicine, Pharma

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