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HPLC (High Performance Liquid Chromatography) I: Basics - 101

  October 04, 2017  
CfPA-The Center for Professional Advancement, Online Live
November 8, 2017 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 HPLC or who perform routine testing using HPLC. 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 HPLC experience, laboratory technicians who wish to gain a better understanding of HPLC theory and its applications, researchers with degrees in other disciplines who need to begin their own HPLC work. This includes: organic synthesis, quality control, and methods developments chemists and various research personnel. 

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

Course Description
This HPLC course is designed to help new users become familiar with all aspects of the HPLC. This 90-minute accredited course will help any new user get started by giving practical information on HPLC theory, its many modes of operation and how to ensure that the analysis and the HPLC are working properly. New HPLC 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.

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) II: Method Development
November 9, 2017 • Course ID #2680

HPLC (High Performance Liquid Chromatography) III: Method Development of Peptides and Proteins
November 10, 2017 • Course ID #2681
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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