METTLER TOLEDO invites you to view our latest particle characterization technologies at the American Association of Pharmaceutical Scientists (AAPS) Workshop: Utilization of Process Modeling and Advanced Process Control in QbD based Drug Development and Manufacturing.
Columbia, MD (PRWEB) April 5, 2009 -- Particles play a critical role in drug product quality. Optimization and control of particles ensures Quality by Design (QbD) in solid dosage formulation. Visit our tabletop exhibit at the AAPS Workshop: Utilization of Process Modeling and Advanced Process Control in QbD based Drug Development and Manufacturing to see how FBRM® and PVM® Process Analytical Technologies (PAT) are used to promote faster formulation development, improve process confidence, and control batch-to-batch consistency in manufacturing.
FBRM® tracks tablet, capsule, and granule disintegration and dissolution mechanisms in real time to uncover the root cause of dissolution performance inconsistencies. FBRM® maps dissolution and disintegration throughout the design space to easily identify critical process parameters. FBRM® correlates release inconsistencies to the upstream source of variability including changes in raw materials, granulation inconsistency, or tableting irregularities in milling.
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