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Capillary Electrophoresis: An Introduction

 
  October 23, 2018  
     
 
CfPA-The Center for Professional Advancement, Online Live
January 24, 2019 at 11:00 a.m.–12:30 p.m. (ET)


Who Should Attend?
This online training will be most useful for people with little to no experience with Capillary Electrophoresis (CE) or who perform routine testing using CE. This course will benefit laboratory personnel in many industries including: pharmaceutical – traditional and phytochemical, food, beverage, environmental, chemical, and personal products.

The potential job functions would be entry level laboratory personnel with no CE experience, laboratory technicians who wish to gain a better understanding of CE theory and its applications, researchers with degrees in other disciplines who need to begin their own CE work. This includes: organic synthesis, quality control, and methods developments chemists and various research personnel. 

The departments in companies involved with the use of CE in research/development or quality control/quality assurance should insist their new personnel attend this training.

Course Description
This Capillary Electrophoresis (CE) course is designed to help new users become familiar with all aspects of the CE. 

This 90-minute accredited course will help any new user get started by giving practical information on CE theory and explaining the different modes of operation. New CE users who take this course will be empowered with the tools they need to get a solid start using this analytical tool with its many valuable and versatile analytical uses and applications.

Can't Make this LIVE Webinar? 
Simply select the On Demand option when registering and we will send you the link to view the recorded version.

This course will be available On Demand: January 25, 2019
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Rachel Monsef; Consultant to the pharmaceutical industry

Rachel Monsef is a consultant to the biopharmaceutical industry for analytical and quality control. She has 18 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. Ms. Monsef 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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