Seminar - Mississauga, Ontario, Canada
Pharmaceutical industry is experiencing a growing need to improve performance driven by global competition and the increasing impact of information technology. FDA’s Process Validation Guidance calls for continued process verification which applies to both manufacturing and measurement processes. How to go about this improvement in a systematic, focused and sustainable manner is the question. Fortunately a world-class body of improvement technology exists known as Quality by Design (QbD); a science and data-based approach that builds quality into products and processes during development, validation and operations.
Wednesday, April 29, 2015 (13:00 - 14:00)
Compliance Trainings, Mississauga, Ontario 44813, Canada
Phone: 4169154458
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