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Capillary Electrophoresis Part 4: Validation of Capillary Electrophoresis Methods – Advanced Topic

 
  May 31, 2018  
     
 
CfPA-The Center for Professional Advancement, Online Live
July 25, 2018 at 11:00 a.m.–12:30 p.m. (ET)


Who Should Attend?
This online training will be most useful for pharmaceutical industry personnel who are familiar with CE techniques and who interested validating methods per ICH/FDA guidelines. This course will be helpful to those who are developing methods for later validation, preparing methods to be validated, or reviewing data from validation packages.

The potential job functions would be mid-level laboratory personnel in analytical, quality control and quality assurance positions who work on method validation. This course will give guidelines for implementing regulations while validating methods.

Course Description
This validation course will help with validating CE methods within ICH guidelines, specific examples will be given for cIEF and CE-SDS; however, information applies to all CE techniques. This 90-minute accredited course will give personnel the tools for evaluating methods for validation readiness, validate their methods, and trouble shoot issues within the validation.  

For maximum benefit, the subject matter expert recommends attending the entire 4-part CE training series.
Capillary Electrophoresis (CE) Part 1: Introduction
July 17, 2018 at 11:00 a.m.–12:30 p.m. (ET) • Course ID #2823

Capillary Electrophoresis (CE) Part 2: CZE and CE-SDS
July 18, 2018 at 11:00 a.m.–12:30 p.m. (ET) • Course ID #2821

Capillary Electrophoresis Part 3: Isoelectrofocusing (cIEF)
July 24, 2018 at 11:00 a.m.–12:30 p.m. (ET) • Course ID #2822 

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: July 26, 2018
 
 
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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