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

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

19 Views

12 Oct 2018 - 12 Oct 2018

Event Serial
: ECA10410
Event Type
: Webinar
Contact Person
: Event Manager Send Message
Deadline for abstracts/proposals
: 11 Oct 2018
Organized by
: Compliance4All DBA NetZealous
Venue
: Fremont, California, United States of America

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