This interactive workshop provides up-to-date, relevant and detailed information on the impact of Quality by Design (QbD) on the Development and Validation of tablet manufacturing processes. It will also study the identification and evaluation of Critical Product Attributes and Critical Process Parameters for tablets, and their implications for process control. We develop new concepts including the use of risk and process matrices for risk management. The latest ICH and FDA guidance on Quality by Design and Process Development, published in 2009, will be comprehensively reviewed
Tablet Process Development, Validation and the application of QbD
11 - 12 April 2011, North Brunswick, United States
Introduction
Venue
CCIT, The Technology Centre of New Jersey
CCIT, The Technology Centre of New Jersey, 675 US Highway One, North Brunswick, 08902, United States
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Organised by
PharmaTraining Ltd
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