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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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March 26, 2012 |
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Center for Professional Innovation & Education (CfPIE), Los Angeles, CA
Aug. 6 & 7, 2012
This two-day course is designed for all scientists (managerial and laboratory), regulatory affairs and compliance personnel who are active in pre-clinical studies and in other laboratory settings. The course will be of most benefit to professionals whose job function necessitates the generation, evaluation, assurance and submission of data from pre-clinical studies. By the end of the course, attendees will have a strong understanding of the fundamental compliance requirements for current Good Laboratory Practices (GLP), and will be able to apply compliance protocols in all efforts aimed at generating regulated data for evaluation by the US FDA and other global regulatory agencies. All participants will gain a fundamental understanding of the regulations and the need for rigorous implementation. Special attention will be given to incorporating proactive thinking and a robust compliance regimen in all scientific matters. The consequences of non-compliance will also be examined.
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Organized by:
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Center for Professional Innovation & Education |
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Invited Speakers:
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Contact info@cfpie.com for a list of course instructors
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Deadline for Abstracts:
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n/a
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Registration:
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http://www.cfpie.com/showitem.aspx?productid=112&source=hummolgen
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E-mail:
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info@cfpie.com
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WWW: Kai Garlipp,
Frank S.
Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved.
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