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GlobalCompliancePanel, Online
March 3, 2010
Every well run pharmaceutical manufacturing facility has established a team of its personnel who will be responsible for hosting an FDA inspection, providing assistance as needed, and monitoring their activities. This program is a vital preparation for the inevitable FDA inspection. It will help sharpen your skills and prepare team members for the inevitable day of inspection This presentation will prepare a manufacturer for FDA inspections, suggest methods for managing the inspection, and assure a smooth and pleasant inspection.
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Organized by:
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GlobalCompliancePanel |
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Invited Speakers:
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James Harris
President, James Harris Associates Inc.
Dr. Harris has over 25 years of senior level pharmaceutical industry experience. Following this and for the past 15 years, he operated a global consulting firm that provided guidance to firms in over 60 countries around the world. During his tenure in the pharmaceutical industry, he was very active in industry groups. He served on the PMA's Validation Advisory Committee and was chairman of the Computerized Systems Advisory committee where he wrote the original guideline on computer validation and negotiated its acceptance with FDA. While consulting, he and his consulting teams have assisted numerous clients around the world with validation of their manufacturing processes.
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Deadline for Abstracts:
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March 2, 2010
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Registration:
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Wednesday, March 3, 2010
10:00 AM PST | 01:00 PM EST | | | Live live online training only for one participant | | |
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| | | Corporate Live 4 to 10 participants from a single location (For multiple locations contact Customer Care) | | |
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E-mail:
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webinars@GlobalCompliancePanel.com
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