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CfPA - The Center for Professional Advancement, 90 Minute Accredited Online Training
December 6, 2012 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend
This online training course will benefit professionals in the following industries:
Pharmaceutical, Biopharmaceutical, Vaccine, Cellular/Gene/Tissue Therapy, and other Biological Products Industries.
The training will be of benefit to all persons whose span of responsibility includes compliance with Good Manufacturing Practice regulations including, but not limited to Scientists and other professionals in Compliance, Development, Manufacturing and Production, Quality Assurance, Quality Control, Regulatory Affairs, and Validation. The course will also be of benefit to supervisors in GMP areas and to mid-level and senior managers whose span of responsibility includes functional areas which require CGMP compliance. Description
This course will be available On Demand: December 7, 2012
This intensive 90-minute accredited online training course focuses on exploring key differences between the European Union European Medicines Agency (EU EMA) and United States Food and Drug Administration (USFDA) regulations and regulatory agency expectations, and upon learning how to deal effectively with such regulatory diversity. Lack of knowledge in this area causes many regulatory problems for companies developing or selling products internationally. Attend or view this course and get knowledge you need to prosper in this everchanging, highly-regulated global environment.
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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.
In his more than 25 years working with the US, European, Canadian pharmaceutical, biopharmaceutical, and biologics industries Dr. Tom Pritchett has gained considerable experience in most 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 and for officials, regulators, and industry professionals of countries in the Gulf Cooperation Council (GCC). Dr. Pritchett is also an active industry consultant and the co-founder/publisher of the newsletter BioQuality (www.bioquality.biz).
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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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