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Pharmaceutical Compressed Air - Quality GMP Standards and Requirements

Thursday, May 11, 2017 at 10:00AM - 1:00PM

Online Event

  • May 2017

    11 Thu

    10:00AM

  • May 2017

    11 Thu

    1:00PM

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Pharmaceutical Compressed Air - Quality GMP Standards and Requirements

Thursday, May 11, 2017 at 10:00AM - 1:00PM

Fremont, CA

No tickets available

Description
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. Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the system.

Objectives Of The Presentation
  • Compressed Air - Importance of Quality
  • Pharmaceutical Compressed Air System Design
  • Contamination Types and Sources
  • Contamination Prevention
  • International GMP Testing Standards
  • Testing Methods and Specifications
Why Should you Attend
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.

A detailed description of a typical pharmaceutical compressed air system with its individual components is provided. Engineering schematics are included. All component functions are detailed with recommendations as to which component type is considered optimal.

The four contamination sources in compressed air are discussed. These are:
  • solid particulate
  • water content
  • total oil content
  • microbial bioburden
For each of these, the presentation will discuss cause and effect. Suggestions are also provided for prevention of the contamination.

Finally, a compilation of all FDA/EU GMP Guidances, USP/EP and ISO air standards are presented. Sampling and testing methodology for each of these specifications is discussed.

Who will Benefit
This webinar will provide valuable assistance to all personnel in:
  • Quality Assurance
  • Environmental Monitoring
  • Microbiology
  • Manufacturing
  • Validation
  • Engineering & Maintenance.


For Registration

http://onlinecompliancepanel.com/webinar/PHARMACEUTICAL-COMPRESSED-AIR-502789/MAY-2017-ES-EZEVENT


Note: Use Promo code WE3PL and get 10% off on registration (Valid till MAY 31st 2017)

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