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 QualityPharmaceutical Compressed Air System DesignContamination Types and SourcesContamination PreventionInternational GMP Testing StandardsTesting Methods and Specifications
Who Will Benefit: This webinar will provide valuable assistance to all personnel in Pharmaceutical Manufacturing and Compounding Pharmacies:Quality AssuranceEnvironmental MonitoringMicrobiologyManufacturingValidationEngineeringMaintenance
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: +1-800-447-9407Email: support@compliance4All.com