Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel 2012

  • 24 Jul 2012
  • Webinar

Description

Topics
  • Audit preparation
  • Examine key elements of an API audit
  • Audit itself
  • Opening Session
  • Discussion of findings
  • What to look for?
  • Closing Meeting
  • Suggestions and experience
  • Who should attend openning and closing sessions
  • Who should participate in audit
  • Follow-up Actions
  • Audit Reports
  • Follow-up Audits
  • Agreed upon Schedules
Who should Attend
  • Supervisors and Managers in Quality
  • Supervisors and Managers in Manufacturing
  • Maintenance Supervisors and Managers
  • Engineering
  • Warehousing and Materials Management Supervisors and Managers

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Important

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Event Categories

Education: Training
Health & Medicine: Healthcare, Medical device, Pharma

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