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CfPA-The Center for Professional Advancement, 90 Minute Accredited Online Training
December 11, 2015 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend?
This online training will benefit professionals in the Pharmaceutical, Biopharmaceutical, Vaccine, Cellular/Gene/Tissue Therapy, and other Biological Products Industries whose activities include compliance with Current Good Manufacturing Practice.
Professionals in Compliance, Quality Assurance, Quality Control, Regulatory Affairs, Manufacturing and Production, R&D, and other departments having to do with regulatory compliance will benefit from this online course. 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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| Thomas J Pritchett, Ph.D., Consultant |
Thomas J Pritchett, has worked with the US, European, and Canadian pharmaceutical, biopharmaceutical, and biologics industries for more than 25 years, during which he has gained considerable experience in regulatory and technical aspects of Quality Assurance, Quality Control and CGMP Compliance for both investigational and marketed products. He is also an experienced teacher, and has been directing courses for the Center for Professional Advancement since 1995. In addition, Dr. Pritchett has provided training sessions for the US FDA, for regulators and industry professionals in the Gulf Cooperation Council (GCC) and at the National Institutes of Health. Dr. Pritchett is also an active industry consultant and the co-founder/publisher of the newsletter BioQuality (www.bioquality.biz). He sits on the editorial advisory board of BioProcess International.
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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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