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HPLC (High Performance Liquid Chromatography) III: Method Development of Peptides and Proteins

  October 04, 2017  
CfPA-The Center for Professional Advancement, Online Live
November 10, 2017 at 11:00 a.m.–12:30 p.m. (ET)

Who Should Attend?
This online training will be most useful for people with some HPLC experience who are interested in improving their HPLC methods or personnel who are developing new HPLC methods for Proteins: Biopharmaceuticals, food sciences or any other industry analyzing proteins would be of interest.

The potential job functions would be entry to mid-level laboratory personnel with some HPLC experience, or laboratory personnel with degrees in other disciplines who need to start developing HPLC methods for proteins.  

The departments in companies involved with the use of HPLC in research/development or quality control/quality assurance should insist their personnel attend if they are not being trained in-house or as a supplement to their in-house training.

Course Description
This 90-minute accredited course will include discussions of theory of SEC, Reversed Phase, Ion-Exchange, Hydrophobic Interaction and Protein affinity Chromatography. It will also give basic starting points on method development and method evaluation of these methods. The course is designed to give personnel with some HPLC experience a broader scope for how to use this invaluable analytical tool.

Maximize learning and minimize expense! 
Register for all 3 parts and save $150 OR take any one as a stand-alone course.
Attend this course and its Companion Courses:
HPLC (High Performance Liquid Chromatography) I: Basics - 101
November 8, 2017 • Course ID #2679

HPLC (High Performance Liquid Chromatography) II: Method Development
November 9, 2017 • Course ID #2680
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Rachel Monsef; Consultant to the pharmaceutical and biopharmaceutical industries

Rachel Monsef is an analytical chemist in the pharmaceutical industry who has 17 years’ experience working in Analytical and Quality Control for all stages of drug development. She has been responsible for method development, method qualification, method validations, assay transfer, characterization work, and stability studies. Ensuring GMP compliance with data integrity has always been within the realm of these responsibilities. She has used many different software interfaces and data storage systems that had to comply with 21CFR11. Through her consulting she has gained much experience with remote data review ensuring that data integrity is present for her client. She has previously worked for Seattle Genetics and Alder Biopharmaceuticals. She is currently a Quality Control Consultant at Alder Biopharmaceuticals.

Ms. Monsef received her Bachelor of Science in Chemistry from the University of Washington.
Deadline for Abstracts: n/a
Registration: Please click here for registration information.
E-mail: jmorbit@cfpa.com
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