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CfPA-The Center for Professional Advancement, 90 Minute Accredited Online Training
April 21, 2015 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend?
This webinar will benefit the following departmental personnel in the Pharmaceutical, Biotechnology, Diagnostics, Drugs, Cell Therapy, Biologics and Medical Device industries:
• Quality Control
• Manufacturing/Production
• Senior Management
• Regulatory Affairs
• Quality Assurance
• Compliance
• Design Engineers
• Facility, Maintenance and Engineering
• Test Contractors Course Description
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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 (CEO/Founder), Pharmabiodevice Consulting LLC |
Charity Ogunsanya has more than 24 years of extensive experience within the Biologics, Pharmaceuticals, Radiopharmaceuticals, Biotechnology, Cell Therapy, Diagnostics, Drug and Medical Device Industries and has been the Microbiology, Sterility Assurance, Contamination Control, Aseptic processing, Quality Control subject matter expert 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 Biodefense. She is the CEO/Founder of Pharmabiodevice Consulting LLC. The consultancy provides Quality and Compliance consultancy/support to Biologics, Pharmaceuticals, Cell Therapy, 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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This 90-minute accredited training will offer a basic understanding of the Clean room regulations, design, classification, sources and types of particles. The different classifications and limits for Clean room particles as it applies to various regulatory bodies’ and requirements will be addressed. Discussions will include the types of micro-organisms, routine monitoring processes, typical mitigation steps in ensuring an effective contamination control through monitoring, sanitization, cleaning, personnel training, gowning, and material, product and personnel flow during a Clean room operation.