Auditing Analytical Laboratories for FDA Compliance 2017

  • 20-21 Nov 2017
  • Manila, Philippines

Description

Topics
  • Reviewing Documentation
  • GMP Regulations that Apply to Analytical Laboratories
  • Auditing Styles and Structures
  • Advance Preparation for the Audit
  • What to look for while doing a Walk-Through
  • Equipment and Laboratory Instrument Qualification
  • Following through on the Audit
  • Other Regulations and Standards, including ISO 17025
Who should Attend
  • Supervisors and Analysts in Quality Control Laboratories and Quality Assurance groups
  • External and Internal Auditors
  • Personnel Responsible for Selecting Contract Testing Laboratories
  • Supervisors and Analysts in Contract Testing Laboratories
  • Consultants

Past Events

Important

Please, check "Auditing Analytical Laboratories for FDA Compliance" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance, Quality assurance
Health & Medicine: Medical laboratories
Science: Laboratories

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