What you need to know to Meet FDA and International Quality Standards
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Website https://www.compliance4all.com/control/w_product/~product_id=502305LIVE?channel=ourglocal_Feb_2019_S |
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Category Pharmaceutical Compressed Air, Quality Standards, Manufacturing, uses of compressed air, Compressed Air System Design, GMP Testing Standards, Environmental Monitoring, Pharmaceutical Manufacturing
Deadline: February 17, 2019 | Date: February 18, 2019
Venue/Country: Online, U.S.A
Updated: 2018-12-07 15:00:39 (GMT+9)
Call For Papers - CFP
Overview:Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the system.Why should you Attend: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.Areas Covered in the Session:Pharmaceutical Compressed Air System DesignContamination Types and SourcesContamination PreventionInternational GMP Testing StandardsTesting Methods and SpecificationsWho Will Benefit:Quality AssuranceEnvironmental MonitoringMicrobiologyManufacturingValidationEngineeringMaintenanceSpeaker 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.Event Fee: One Dial-in One Attendee Price: US $150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14gmail.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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