759 QbD for the Development of Drug Release and Dosage Systems

Thursday, November 7, 2013: 3:15 PM
Plaza A (Hilton)
Description:
This session invites papers pertaining to the development, performance, and robustness of drug delivery systems and dosage forms. Topics involve the statistical design of experiments and analyses relevant to the above criteria, for optimizing formulation design, process development, manufacturing, and analytical metholodologies.

Sponsor:
Pharmaceutical Discovery, Development and Manufacturing Forum

Chair:
Padma Narayan
Email: PNarayan@dow.com

Co-Chair:
Jason Mustakis
Email: Jason.Mustakis@pfizer.com

- indicates paper has an Extended Abstract file available on CD.


3:15 PM
(759a) Simulation Study Comparing Oil Emulsion Particle Size Distributions On a Performance Basis
Stephen D. Stamatis and Lee E. Kirsch

3:40 PM
(759b) Impact of Hpmcas Polymer Properties On the in Vitro Performance of Spray Dried Dispersions – A Quality By Design Approach
William Porter III, Robert Schmitt, Oliver Petermann, Steven Guillaudeu, Meinolf Brackhagen and Matthias Sprehe

4:05 PM
(759c) Principal Component Analysis for Pharmaceutical Process and Product Characterization:Case Study From Immediate and Controlled Release Tablet Manufacturing
Huiquan Wu

4:30 PM
(759d) Dissolution of Different Commercial Aspirin Tablets Using a Novel Off-Center Paddle Impeller (OPI) Dissolution Testing System
Yang Qu and Piero M. Armenante
File available
4:55 PM
(759e) The Effect of Blend Shearing and Compression On Dissolution Dynamics for Immediate Release Tablets
Gerardo Callegari, Tarek Awad, Yifan Wang, Pallavi Pawar, Wiphusanee Dendamrongvit, German Drazer, Fernando J. Muzzio and Alberto Cuitino

5:20 PM
(759f) Design Space Approach to Continuous Manufacturing of Drug Loaded Terapeutic Films
Phong Huynh and Paul Takhistov
See more of this Group/Topical: Pharmaceutical Discovery, Development and Manufacturing Forum
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