What you need to know to Meet FDA and International Quality Standards

MessageThis Webinar is over
Date Oct 12, 2018
Time 10:00 AM to 11:00 AM
Cost 150.00
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.

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. 

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: This webinar will provide valuable assistance to all 

personnel in Pharmaceutical Manufacturing and Compounding Pharmacies:
Quality Assurance
Environmental Monitoring

Speaker Profile:
Roger Cowan is the founder and owner of R Cowan Consulting Services 

LLC, a consulting company specializing primarily in the area of 

pharmaceutical contract manufacturing. He has 37 years experience in 

pharmaceutical quality assurance and manufacturing. In his career, Roger 

has held various manager / director positions in Quality Assurance, QC 

Laboratory, Technical Services Validation, Manufacturing, and Clinical 

Supply manufacturing and distribution.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com


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