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

Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries

  January 06, 2012  
Center for Professional Innovation & Education (CfPIE), Los Angeles, CA
May 23 & 24, 2012

This course will be of benefit to pharma, medical device, and biotech professionals who manage documents for all therapeutic product development and marketing activities (including pre-clinical, clinical, QA, and regulatory functions). This two-day course is also valuable for QA auditors who need to understand what constitutes sound documentation and documentation management.  Upon completion of this course participants will be able to increase your ability to implement efficient practices that meet full GLP/GMP/ICH, ISO, and other regulatory requirements.
Organized by: Center for Professional Innovation & Education
Invited Speakers: Contact info@cfpie.com for a list of course instructors
Deadline for Abstracts: n/a
Registration: http://www.cfpie.com/showitem.aspx?productid=027&source=hummolgen
E-mail: info@cfpie.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- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.