2010 Annual Meeting

Area: Pharmaceuticals

Chair

Joe Hannon, DynoChem Inc

Co-Chairs

Partha Mudipalli, Cephalon, Inc.

Sessions sponsored

Application of Green Chemical Engineering Approaches to Improve Sustainability in Pharmaceutical Manufacturing
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Applications of Continuous Processing in Manufacture of Drug Product
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Applications of Continuous Processing in Manufacture of Drug Substance / API
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Applications of Continuous Processing In the Pharmaceutical Industry
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Bioseparations / Downstream Processing of Biopharmaceuticals 1
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Bioseparations / Downstream Processing of Biopharmaceuticals 2
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Characterization and Processing Solutions for API and Drug Product
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Crystallization of Pharmaceutical and Biological Molecules 1: In Honour of the Late Dr. Jeff Wei of Eli Lilly
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Crystallization of Pharmaceutical and Biological Molecules 2: In Honor of the Late Dr. Jeff Wei of Eli Lilly
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Integrated API and Drug Product Development
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Poster Session: Pharmaceutical Engineering
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Quantitative Use of Particle Characterization Data for Process Modelling
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Reaction Engineering in API Synthesis
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Sessions co-sponsored

Applications of Multivariate Data Analysis in Pharmaceutical Process Development
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Applications of PAT in a Manufacturing Setting
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Bio and Pharmaceutical Process Design
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Challenges Facing CMC Organizations in the Changing Business and Regulatory Environment
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Characterization of Engineered Particulate Systems for Pharmaceutical Active Ingredient Delivery
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Engineered Composite Particulate Systems for Pharmaceutical Active Ingredient Delivery
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Food, Pharmaceutical and Bioengineering Plenary Session
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Mixing and Scale-up/Scale-Down Strategies for the Production of Biopharmaceuticals
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Mixing and Segregation of Particulates I
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Mixing in Multi-Phase Systems II
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Model Based Integrated Design of Pharmaceutical Drug Product and Process
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Model Based QbD in Drug Substance or Drug Product
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Particle Formation and Crystallization Processes From Liquids, Slurries, and Emulsions I
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Particle Formation and Crystallization Processes From Liquids, Slurries, and Emulsions II
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PAT for Crystallization Development and Manufacturing
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QbD Topical Plenary Session
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Quality by Design in Generic Drug Development
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Quality-by-Design (QbD) Round Table Discussion Session: An Integrated and Science-Based Approach for Quality by Design (QbD) Implementation in Pharmaceutical Industry
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Quality-by-Design (QbD): Techniques for Quality Risk Analysis and Management Over the Product Life Cycle
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Reaction Engineering in Pharmaceuticals and Fine Chemicals
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Scale-up of Pharmaceutical Manufacturing Processes: Toward a QbD Approach
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TI Application of Quality by Design In API Process Development
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TI Application of Quality by Design in Drug Product Process Development
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