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Northeast Regional Forum September 2017
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Thursday, September 28, 2017

University of Massachusetts Boston (UMB) 

 

 




Managing Process-related Impurities in Biological Products


Thank you to everyone who participated in the inaugural Northeast Regional Forum!
Save the date for our next program: "Assessment of Criticality of Quality Attributes for Biotherapeutics"
on Wednesday, May 2, 2018 at the Biogen campus in Cambridge, MA.

 

The Northeast Regional Forum is committed to bringing job-relevant education to the local biopharmaceutical and biotechnology community. These programs are dedicated to facilitating the sharing of information and best practices in order to advance scientific knowledge across industry, academia, and regulatory agencies. This full day program will feature presentations on managing process related impurities in biological products, an interactive panel discussion, roundtable discussions, and opportunities to network with peers.

 

 

Learning Objectives:

Learn and discuss current challenges, trends, and expectations for process related impurity control and analysis from industry peers and FDA colleagues, with a particular focus on HCP contaminants.

Key areas of discussion will include:

• Process development experience establishing clearance of process-related impurities using immunoassay versus MS approaches.
• Current best practices for HCP analysis by immunoassay.
• Industry approaches for application of MS methods to process related impurity control strategies.

   

Want more information? Check out the "More in this Section" dropdown box at the top of the page!
Or contact CASSS at 510-428-0740 or alingel@casss.org

 


  

 

 

 
 
 
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