Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
May 23 - 24, 2012 - Los Angeles PA US
Center for Professional Innovation and Education, Inc.
Phone: (610) 688-1708
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.