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CfPA - The Center for Professional Advancement, 90 Minute Accredited Online Training
August 15, 2013 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend
This webinar will provide a great resource to suppliers/vendors and users of pharmaceutical grade gases such as cGMP product manufacturers in the design and routine operation of a new or existing gas program in order to meet ISO 8573, USP or FDA requirements. It will specifically be a great resource to personnel in the Pharmaceutical, Biotechnology, Biologics, Drugs, Medical Device, In-vitro Diagnostics industries within the following functions: Quality Control, Quality Assurance, Microbiologist, Chemist, Analysts, Manufacturing, Validation, Facilities, Materials Management, Engineering, Vendors/Suppliers, Regulatory Affairs and all levels of management.
However, if you are already familiar with designing, validating and routine testing of a pharmaceutical gas system, you may recommend this webinar to professionals within the various industries that may require additional knowledge about this topic. Description
This course will be available On Demand: August 16, 2013
This webinar will describe how to design, perform routine testing, and utilize the test data from different types of gas systems such as Nitrogen, Argon and Compressed Gases. This webinar will also provide a step-by-step guidance to a product manufacturer that is planning to install, validate and routinely test a new or modified existing gas system so as to comply with the regulations. This course will also cover topics such as how to set the appropriate gas testing frequency, types of testing to be performed, setting the alert and action levels, utilizing the gas testing results, performing data evaluation, data management, data trending, performing failure, contamination, excursion and out-of-specification investigation and remediation and product disposition by the Quality unit.
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Organized by:
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CfPA - The Center for Professional Advancement |
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Invited Speakers:
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Charity Ogunsanya (Owner/CEO). Pharmabiodevice Consulting LLC
Charity Ogunsanya has more than 23 years of extensive experience within the Biologics, Pharmaceuticals, Radiopharmaceuticals, Biotechnology and Medical Device Industries and has been the Microbiology, Sterility Assurance, Contamination Control, Aseptic processing, Quality Control Subject Matter Expert (SME) for multiple fortune 100 companies. She has a Bachelor of Science degree in Microbiology from the University of Benin-Nigeria and is currently in the Advanced Academic Master’s Biotechnology Program at the Johns Hopkins University with concentration in Biotechnology/Biodefense. She is the CEO/Owner of her consulting firm named Pharmabiodevice Consulting LLC. Her consultancy provides support to Biologics, Pharmaceuticals, Radiopharmaceuticals, Biotechnology and Medical Device Industries.
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Deadline for Abstracts:
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n/a
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Registration:
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Please click here for registration information.
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E-mail:
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sberg@cfpa.com
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