Implementing a Risk-Based Internal cGMP Annual Audit Program 2018

  • 05 Dec 2018
  • Webinar

Description

Topics
  • Avoid complacency from past "good" U.S. FDA/ EU ISO audits
  • Regulatory issues
  • Suggested "Models"
  • Applicable guidance documents
  • A risk-based phased approach
  • Data Sources / Metrics
  • Entropy
Who should Attend
  • Quality Departments
  • Regulatory Affairs Departments
  • Compliance Departments
  • CGMP compliance auditors
  • Engineering Departments
  • Research and Development Departments
  • Production Departments
  • Manufacturing Departments
  • Middle management
  • Senior management

Past Events

Important

Please, check "Implementing a Risk-Based Internal cGMP Annual Audit Program" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Management, Quality assurance
Science: Engineering

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