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Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards - Webinar

  • ID: 4755607
  • Webinar
  • February 2019
  • Region: Global
  • 60 Minutes
  • World Compliance Seminar
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This webinar will take you through the primary sources of compressed air contamination. It will also detail GMP standards and requirements pertaining to compressed air quality. The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without product contamination. Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the system as well.
Note: Product cover images may vary from those shown
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  • Compressed Air - Importance of Quality
  • Pharmaceutical Compressed Air System Design
  • Contamination Types and Sources
  • Contamination Prevention
  • International GMP Testing Standards
  • Testing Methods and Specifications
Note: Product cover images may vary from those shown
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  • Environmental monitoring
  • Microbiology
  • Manufacturing
  • Validation
  • Engineering
  • Maintenance
Note: Product cover images may vary from those shown
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