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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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January 17, 2019 |
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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
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Organized by:
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CfPA-The Center for Professional Advancement |
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Invited Speakers:
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| 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.
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Deadline for Abstracts:
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n/a
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Registration:
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Please click here for registration information.
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E-mail:
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Jmorbit@cfpa.com
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WWW: Kai Garlipp,
Frank S.
Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved.
Liability, Copyright and Imprint. |
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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