Writing and Managing SOPs Effectively for GMP Operations 2014

  • 03-04 Jul 2014
  • Mandarin Orchard Singapore

Description

Topics
  • FDA requirements and Expectations
  • Documents including SOPs
  • Determine the needs of new SOP
  • General controls for Documentation
  • Different types of SOPs
  • Determine the responsibility for SOP
  • Organizing information on an SOP
  • Format and writing techniques for an SOP
  • Management Aspects of SOP
Who should Attend
  • Quality Assurance scientists
  • Laboratory Analysts
  • QA/QC Managers
  • QA/QC Mnalysts
  • Inspectors
  • Auditors
  • Manufacturers of Raw Materials and Excipients
  • Pharmaceutical Development and Manufacturing Personnel
  • Contract Laboratory Organization Personnel

Past Events

Important

Please, check "Writing and Managing SOPs Effectively for GMP Operations" official website for possible changes, before making any traveling arrangements

Event Categories

Education: Training
Health & Medicine: Healthcare, Hospitals & Clinics, Internal medicine, Medical technology, Pharma

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