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Routine Analytical Methods for BioPharmaceuticals: FREE WEBINAR

 
  January 18, 2018  
     
 
CfPA-The Center for Professional Advancement, FREE WEBINAR
January 24, 2018 at 10:00 a.m.–10:30 a.m. (ET)


Who Should Attend?
This FREE informational webinar will provide insight to bio-pharmaceutical personnel on the purpose of routine test methods used within an analytical program. This webinar will help with understanding and interpreting data from each method discussed. Additionally you will learn how each method helps support product quality.

It will be valuable to the following professionals:
  • Quality Control, Quality Assurance
  • Analytical Scientist
  • Research Associates
  • Engineers and Administrators working in analytical development, 
     Product Development, Manufacturing, Validation, Formulation, and 
     Pre-formulation groups, though any inquiring minds within this 
     industry are welcome to join

Course Description
This 30-minute FREE informational webinar is intended to be an overview of routine methods commonly used for bio-pharmaceuticals and the reportable data that comes from each method.

  • Method types that will be discussed during course are UV-VIS, SEC, Reversed 
     Phase, SDS-PAGE/CE-SDS, IEF Gels/cIEF and ELISA.

• For each method will discuss 
     – Reportable data from method
     – Why method is important 
     – How method fits into product quality

Can’t attend LIVE? Register anyway and we’ll send you a link to the webinar recording afterwards.

For complete coverage of this subject check our website for: 
Biopharmaceutical Analytics: Method Development
March 6-7, 2018 | New Brunswick, NJ | Attend In Person or Virtually
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Rachel Monsef, Consultant to the pharmaceutical and biopharmaceutical industries

Rachel Monsef is a consultant to the biopharmaceutical industry for analytical and quality control. She has 17 years’ experience working with many types of assay for all stages of drug development. She has been responsible for method development, method qualification, method validations, assay transfer, characterization work, and stability studies. She has also worked with manufacturing groups to develop and perform assays to support their efforts. She has previously worked for Seattle Genetics and Alder Biopharmaceuticals and is currently consulting for Alder Biopharmaceuticals. 

 


 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: jmorbit@cfpa.com
 
   
 
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