Institute for International Research

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Use and Importance of Dissolution in Generic Development Including IVIVC
10:30 am
Eric Beyssac, PhD, Faculty of Pharmacy, ERT CIDAM, Universite d'Auvergne, Clermont-Ferrand, France

Quality by Design: Understanding the Correlation between Drug Dissolution Behavior and Key Formulation Parameters
11:15 am
Yu Lu, Scientist II, Vertex Pharmaceuticals

Interactive Panel Discussion: Dissolution Testing and Specification Setting: Where Does Dissolution Testing Add Value?
12:00 pm
David Fortunato, Scientist, Johnson & Johnson PRD, LLC.

Flow Through Dissolution Testing for Low Dose Products
1:45 pm
Samir Haddouchi, Lab & Project Manager, SPS Pharma Services

Challenges in Developing a Robust Dissolution Method for Efficient Formulation Development
9:45 am
Stephen P. Mayock, Senior Manager, Catalent Pharma Solutions

Dissolution from Non-oral Dose Rorms: Implants, Injectables, Stents and Suppositories
11:00 am
Anthony Palmieri III, Ph.D., Assistant Professor of Pharmaceutics, College Of  Pharmacy, University of Florida

Using Bio-Relevant Media for In Vitro Testing to Assess Dosage Form Performance In Vivo as a Risk Management Tool
11:45 am
Jianmei Kochling, PhD, Group Leader, Vertex Pharmaceuticals

New GI Dissolution Testing to Demonstrate Bio- Equivalence
3:30 pm
Lyn Hughes, PhD, Senior Scientist, Process Solutions, Rohm and HAAS Research Laboratories