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


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Who should attend?

Microbiology Manufacturing Validation Engineering

Details

Overview:
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
Microbiology
Manufacturing
Validation
Engineering
Maintenance

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

Prices

One Dial-in One Attendee Price: $150.00

Contact

Event Manager
support@compliance4all.com

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