Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
Berlin, Germany, 19.04.2010 - 20.04.2010

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) should attend this course. 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.

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