Pharmaceutical Compressed Air – Quality GMP Standards and Requirements

MessageThis Webinar is over
Date Aug 2, 2018
Time (1:00 PM - 2:00 PM )
Cost 15070.00
Online
Compressed air is often overlooked as a potential source of clean room and product contamination. This webinar will give you an understanding of the different types of contamination inherent in compressed air and how to prevent each from affecting your particular system.

Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.

The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without contamination of the product.

Areas Covered in the Session :
  • Compressed Air – Importance of Quality
  • Pharmaceutical Compressed Air System Design
  • Contamination Types and Sources
  • Contamination Prevention
  • International GMP Testing Standards
  • Testing Methods and Specifications

Who Will Benefit:
  • Quality Assurance Departments
  • Environmental Monitoring Departments
  • Microbiology Departments
  • Manufacturing Departments
  • Validation Departments
  • Engineering Departments
  • Maintenance Departments

 


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