Session 710 - PAT Implementation in Formulation Development


Pharmaceuticals
Session 710 - PAT Implementation in Formulation Development
The implementation of cutting edge analytical techniques (such as spectroscopy, and other in-situ methods) within pharmaceutical development is important in developing scientifically sound correlations between process conditions and quality product attributes. This session focuses on experimental and theoretical case studies in the areas of process analytical technology focusing on formulation design, process development, modeling of unit operations, scale-up, and advanced process control for parenteral and oral dosage forms.
Chair:	Nancy E. Sever
CoChair:	Padma J. Narayan
	710a	Applications of NIR In Blend Monitoring and beyond: Case Studies from Development Nancy E. Sever
	710b	Optimization and Scale-up of High Shear Wet Granulation Processes Using Lasentec Fbrm and Pvm In-Situ Particle Characterization Zane Arp, Benjamin Smith, Des O'Grady
	710c	Characterizing In-Situ Particle Disintegration Mechanisms to Correlate Formulation Conditions to Tablet Dissolution Profiles Des O'Grady, Eric Dycus, Eric J. Hukkanen, Jeff Seely
	710d	High Throughput Product / Process Monitoring and Control Using Automated Td-NMR Technology Supriyo Ghosh
	710e	A Model-Based Framework for Systematic Product Quality Monitoring and Control Ravendra Singh, Krist V. Gernaey, Rafiqul Gani
	710f	Towards a Robust, Greener API Process Via Cooling Crystallization Evelina Kim, James Marek

Pharmaceuticals