Conference Materials

Program

“Right, First Time” Concept & Workflow Reengineering Preformulation and Formulation Studies

Challenges of physico – chemical characterization of API

Challenges of the first sterile i.v. reference Formulation

Early in–silico & in-vitro prediction of oral drug absorption and Implication on formulation development

Automated drug – excipient compatibility studies

Drug-Excipient Galenical Screening Program for the development of robust and Six Sigma quality tablet formulations

F-CAD: Formulation Computer-Aided Design

Accelerated stability studies and prediction of Six Sigma tablet formulation, ready for the market.