home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
  HUM-MOLGEN -> Events -> Courses and Workshops
Search  -  prev / next
 
 

Good Laboratory Practices (GLP)

 
  January 17, 2019  
     
 
CfPA-The Center for Professional Advancement, New Brunswick, NJ
June 19-21, 2019


Who Should Attend?
This course is intended for all management within industry, government, academia and/or contract biological testing facilities especially:
  • Scientists
  • Regulatory/Compliance personnel
  • Quality Assurance staff
  • Those newly assigned GLP responsibilities
  • More experienced personnel needing to update their knowledge

Course Description
The main intent of this course is to review the requirements imposed by Good Laboratory Practices (GLP) regulations for facilities engaged in toxicology and product safety testing, primarily in animals and biological test systems. The responsibilities and functions of management including the Study Director, Principal Investigator and the Quality Assurance Unit (QAU) will be covered. Various procedures for meeting the requirements of the regulations will be presented.

The lectures will be supplemented by a question and answer session conducted by the Faculty and by workshops involving problem-solving exercises. The course will concentrate on OECD and FDA Good Laboratory Practices and their application. This will include recent developments regarding multi-site studies and their practical interpretation.

Emphasis will be placed on the practical implementation of GLP and discussion including problems that the participants bring to the course. 

Maximize Your Learning!
Attend this course and its Companion Courses:
GLP and Quality Assurance: Developing a GLP Compliant QA Program
June 24-25, 2019 • New Brunswick, NJ • Course ID #2564

GLP Study Director
June 26-27, 2019 • New Brunswick, NJ • Course ID #2136
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
Philip Withers, GLP training and compliance consultant

Philip Withers was Director of Quality Assurance at MDS Pharma Services in France and has been involved in preclinical QA for over 35 years. For 25 years he worked in non-clinical contract laboratories in England and France where he set up the quality assurance programme worldwide. Mr. Withers is a member of the organising committee of SoFAQ (the French national QA society), past chairman of the multi-site working party and senior editor of the Quality Assurance Journal. He has presented many papers at international QA meetings and has been involved for several years in developing a variety of training programmes nationally and internationally including OECD training workshops.

Fourteen years ago he created his own GLP training and compliance consultancy.

 


 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: Jmorbit@cfpa.com
 
 
   
 
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
 
 

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995-2019 HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.