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CE Pharm 2007Oct 14 - 18, 2007
Mark Your Calendar!

August 17, 2007 -
Abstract deadline to be considered for oral presentation.

September 21, 2007 -
Abstract deadline to be considered for poster presentation.

September 21, 2007 -
Final deadline to submit last minute orals and posters for inclusion in the Final Program
(Note: some lecture submissions may be included as oral presentations in "Late-breaking" sessions)

CALL FOR ABSTRACTS

Abstract Submissions Are Now Closed
The Organizing Committee invites pharmaceutical scientists from industry, government regulatory agencies and academia to submit abstracts on their current work by August 17, 2007 to be considered for an oral presentation. September 21, 2007 is the deadline for poster abstract submission.

Notification of acceptance of abstracts for oral presentations will be sent by email and the Symposium Web site will be updated accordingly. Abstracts will be posted on this Web site for review prior to and after the conclusion of the meeting.


 

 

 

CE Pharm 2007

 

The goal of this Symposium is to provide a forum for the discussion of recent developments in CE analysis of protein, nucleotide and small molecule pharmaceuticals. The presentations and workshops will be devoted completely to practical concerns to strengthen the use of CE within the biotechnology and pharmaceutical industries. Applications will highlight uses of CE in various areas of product development including high throughput screening, formulation studies, process development, product characterization and validated lot release and stability testing. The Symposium will feature presentations from leading experts within the industries and the regulatory agencies (FDA, Health Canada). The workshops will allow for open discussions of specific techniques and/or applications including protein analysis, carbohydrate analysis, CE/MS, oligonucleotide and chiral separations as well as validation of CE assays for product release. Specifically, two workshops will focus on the implementation of assays, including assay troubleshooting, assay transfer, and instrument qualification (IQ/OQ/PQ).

 
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