SPI USA, Inc, Frankfurt, Germany
September 25 - 26, 2006
This seminar is right for you if you are responsible for acheiving and maintaining a state of compliance with the FDA and international CGMP requirements; you are personnel associated with supply companies; you are a professional responsible for compliance, regulatory affairs, project planning, technology transfer, QA/QC, R&D or manufacturing.Be a part of this seminar by engaging in round table discussions and case studies. Learn effectively in small class sizes from lecturers with years of hands on experience. Some of the topics covered include: CGMPs and the FDA, Prevention of Contamination, Fundamentals & Essentials of Validation, Inspections & Investigations, as well as Recent FDA Developments. In addition, a half-day presentation comparing EU versus US CGMPs will be performed by Dr. Colman Casey.
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