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GLP and Quality Assurance: Developing a GLP Compliant QA Program

 
  January 17, 2019  
     
 
CfPA-The Center for Professional Advancement, New Brunswick, NJ
June 24-25, 2019


Who Should Attend?
The participants in this course will already know the basics of GLP. The course is designed for those who wish to master how to implement and maintain a GLP QA function. The course explores quality issues within preclinical GLP and provides an opportunity for experienced personnel to update their competencies. Participants may come from:
  • Life-Science Industries
  • Academia
  • Government
  • Contract Testing Facilities

Course Description
This 2-day intensive course will explore the activities of a Quality Assurance department when auditing or inspecting studies and facilities for GLP compliance. All aspects of QA work will be discussed including; the preparation of planning documents, review of protocols and SOPs, inspection of facilities and processes, performance of inspections of on-going phases and the audit of final reports. The presenter will particularly consider the rationale to apply when developing and implementing a QA audit & inspection program. 

Consideration will be given to the role of QA vis-à-vis computerized systems. The reference materials will be the FDA and OECD Good Laboratory Practice Regulations and the series of monographs of the OECD relating to the interpretation of these GLP principles. Time will also be given to the setting up of quantitative techniques for the measurement of Quality, enabling participants to follow the compliance level within laboratories. Presentations will be supplemented with many interactive case studies, problem solving experiences and workshops. 

Emphasis will be placed on the various options available for meeting regulatory requirements.

Maximize Your Learning!
Attend this course and its Companion Courses:
Good Laboratory Practices (GLP)
June 19-21, 2019 • New Brunswick, NJ • Course ID #545

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
 
 
   
 
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